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For customers who do not have access to a Luminex instrument or for
other reasons would rather not perform the genotyping analysis themselves,
Marligen offers Signet™ Genotyping Testing Services. Send us your
DNA samples, buccal swabs, blood or other specimens, and Marligen will
prepare the samples, run the assays of your choice, and supply you with
the data and a genotyping report.
Download the full list of panels for
Testing Services. If you are interested in testing combinations of SNPs
contained within several of our Signet™ Genotyping Panels please
contact technical support with
more details.
Request a Genotyping
Testing Services Quote >>
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| Catalog #11727-000 |
| RefSNP or Description |
Gene (Abr) |
AA Change/Desc |
Base Change |
| rs1800795 |
IL6 |
Promoter Variant |
G-174C |
| rs328 |
LPL |
Ser447Stop |
C1421G |
| rs1801131 |
MTHFR |
Glu429Ala |
A1298C |
| rs4332 |
ACE |
Intronic Variant |
C547T |
| rs1801133 |
MTHFR |
Ala222Val |
C677T |
| rs5128 |
APOC3 |
3'UTR |
C3238G |
|
|
| Catalog #11728-000 |
| RefSNP or Description |
Gene (Abr) |
AA Change/Desc |
Base Change |
| rs234706 |
CBS |
Tyr233Tyr |
C33T |
| GSTM1del |
GSTM1 |
Whole gene deletion |
--- |
| GSTT1del |
GSTT1 |
Whole gene deletion |
--- |
| rs1695 |
GSTP1 |
Ile105Val |
A342G |
| rrs1801282 |
PPAR |
Pro12Ala |
C167G |
| rs1805087 |
MTR |
Asp919Gly |
A2756G |
| rs1800796 |
IL6 |
Promoter Variant |
G-573C |
| rs2228570 |
VDR |
creates a new upstream initiation codon |
C27823T |
| rs708272 |
CETP |
Intronic Variant |
C>T |
|
|
| Catalog #11729-000 |
| RefSNP or Description |
Gene (Abr) |
AA Change/Desc |
Base Change |
| rs1800629 |
TNFa |
Promoter Variant |
G-308A |
| rs1801394 |
MTRR |
Ile22Met |
A66G |
| rs731236 |
VDR |
3'UTR |
C352T |
|
|
| Catalog #11730-000 |
| RefSNP or Description |
Gene (Abr) |
AA Change/Desc |
Base Change |
| rs1544410 |
VDR |
--- |
A>G |
| rs1799983 |
eNOS |
Glu298Asp |
G894T |
| rs1138272 (rs1799811) |
GSTP1 |
Ala114Val |
C341T |
|
|
| Catalog #11731-000 |
| RefSNP or Description |
Gene (Abr) |
AA Change/Desc |
Base Change |
| rs266729 |
ADIPOQ |
--- |
–11377C>G |
| rs1501299 |
ADIPOQ |
Intron |
G276T |
| rs5030980 |
AGRP |
Ala67Thr |
Ala67Thr |
| rs3792267 |
CAPN10 |
Intron |
-43G>A |
| rs5443 |
GNB3 |
Ser275Ser |
C825T |
| rs1143634 |
IL-1b |
Phe105Phe |
T3954C |
| rs8192284 |
IL-6R |
Asp358Ala |
A1510C |
| rs133068 |
MCHR1 |
Promoter Variant |
C>G |
| rs16139 |
NPY |
Leu7Pro |
T106C |
| rs1801282 |
PPARgG |
Pro12Ala |
C167G |
|
|
| Catalog #11732-000 |
| RefSNP or Description |
Gene (Abr) |
AA Change/Desc |
Base Change |
| rs11642466 |
VKORC1 |
Intron |
A>G |
| rs11642603 |
VKORC1 |
Chrom. 16 |
C>G |
| rs2359612 |
VKORC1 |
Intron |
A>G |
| rs4889490 |
VKORC1 |
3' near gene |
G>C |
| rs4889537 |
VKORC1 |
3' near gene |
G>C |
| rs4889599 |
VKORC1 |
5' near gene |
C>T |
| rs7194347 |
VKORC1 |
Chr 16 |
A>T |
| rs7294 |
VKORC1 |
3' UTR |
G>A |
| rs9923231 |
VKORC1 |
5' near gene |
C>T |
| rs9934438 |
VKORC1 |
Intron |
G>A |
|
|
| Catalog #11733-000 |
| RefSNP or Description |
Gene (Abr) |
AA Change/Desc |
Base Change |
| rs1057910 |
CYP2C9 |
Ile359Leu |
A>C |
| rs2860905 |
CYP2C9 |
Intron |
A>G |
| rs3814637 |
CYP2C19 |
5' near gene |
C>T |
| rs4917639 |
CYP2C9 |
Intron |
C>A |
| rs9325473 |
CYP2C9 |
Intron |
A>G |
| rs9332108 |
CYP2C9 |
Intron |
T>C |
| rs17882687 |
CYP2C19 |
ILle19Leu |
A>C |
| rs9332214 |
CYP2C9 |
Intron |
C>T |
|
|
| Catalog #11734-000 |
| RefSNP or Description |
Gene (Abr) |
AA Change/Desc |
Base Change |
| rs1799809 |
PROC |
5’ near gene |
A>G |
| rs2069901 |
PROC |
5’ near gene |
C>T |
| rs2069910 |
PROC |
Intron |
C>T |
| rs12714145 |
GGCX |
Intron |
C>T |
|
|
| Catalog #11735-000 |
| RefSNP or Description |
Gene (Abr) |
AA Change/Desc |
Base Change |
| rs5030838 |
CYP1A1*2A |
Genomic |
3801 T>C |
| CYP1A1*6 |
CYP1A1*2A |
Met331Ile |
1636 G>T |
| rs4987133 |
CYP1A1 |
Ile286Thr |
T>C |
| rs2856833 |
CYP1A1 |
Phe381Leu |
C>A |
| rs1799814 |
CYP1A1 |
Thr461Asn |
2453 C>A |
| rs1048943 |
CYP1A1*2C |
Ile462Val |
2455 A>G |
| rs2278970 |
CYP1A1 |
Ala463Gly |
C>G |
| rs4986826 |
AhR |
Val570Ile |
1768 G>A |
| rs1056836 |
CYP1B1*3 |
Leu432Val |
4326 C>G |
| rs1800440 |
CYP1B1*4 |
Asn453Ser |
4390 A>G |
|
|
| Catalog #117236-000 |
| RefSNP or Description |
Gene (Abr) |
AA Change/Desc |
Base Change |
| rs405509 |
APO E |
5' near gene |
C>A |
| rs3745833 |
GALP |
Met72Ile |
G>C |
| rs8192708 |
PCK1 |
Ile267Val |
A>G |
| rs11622883 |
Near SERPINA13 |
--- |
T>A |
| rs1554948 |
TNK1 |
Leu27Leu |
T>A |
| rs157581 |
TOMM40 |
Phe113Phe |
G>A |
| rs4420638 |
Chromosome 19 |
--- |
G>A |
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Additional Service Testing Information:
Shipment of samples
If you are providing DNA that is ready to analyze, prepare PCR grade
DNA and freeze at –20°C until shipment to Marligen via overnight
carrier on blue or dry ice. (Note: Approximately 25 ng of PCR grade
DNA is required for genotyping.)
If you would like Marligen to provide DNA extraction services, please
call Technical Services at 301-874-4990 x102 to discuss appropriate
sample collection and storage.
The address for shipment is:
Marligen Biosciences Inc. 2502 Urbana Pike
Ijamsville, MD 21754
Attn: Testing Services Manager
Tel 301-874-4990-Ext 102
Please contact Customer Services at 301-874-4990 x107 or by email at customer.service@marligen.com before
sending your samples to alert us that they will be coming and to provide
us with the name of the carrier, the tracking number and the expected
delivery date.
We will notify you when the samples have been received and the contents
of the shipment have been verified against your packing slip. Typically
an electronic copy of a report summarizing the results is transmitted
within 20 business days after receipt of the samples.
Signet™ SNP
Genotyping Kits are also available for you to perform your own
assays on the Luminex® instrument.
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