Gene Variant Report issued
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Lifestyle Genomics Research Centre Ltd.<br />
Plymouth Science Park, 1 Davy Road, Derriford, Plymouth, PL6 8BX , UNITED KINGDOM contact us<br />
SAMPLE PROCESSED BY:<br />
METHOD:<br />
DATA CHECKED FOR ACCURACY BY:<br />
Genome Centre at BARTS and The London School of Medicine and Dentistry<br />
Fluidigm TaqMan probe-based SNP genotyping / Illumina MiSeq, Next <strong>Gene</strong>ration<br />
sequencing<br />
Genome Centre at BARTS and The London School of Medicine and Dentistry<br />
NOTES:<br />
genotype has no risk alleles<br />
genotype has one risk allele<br />
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genotype has two risk allels<br />
either allele can be a risk or be<br />
beneficial<br />
Ctr+F to activate Search Engine: Look up genes, rsids, pathways / traits<br />
SNP RSID INTERPRET ☞ PARENT GENE & VARIANT ⚛ CATEGORY ☤ / PATHWAY ⥹ RISK ALLELES !! cp00035774<br />
rs1613662<br />
The gene encodes a protein that is a<br />
receptor for collagen and plays an<br />
important role in collagen-induced<br />
platelet aggregation and thrombus<br />
formation. Mutations of this gene<br />
can cause a bleeding disorder.<br />
GP6 Pro219Ser <strong>Gene</strong>ral Health / Clotting Factors GG AA<br />
rs9898 rs9898 HRG Pro204Ser <strong>Gene</strong>ral Health / Clotting Factors TT CT<br />
rs5918<br />
C=increased resistance to blood<br />
thinning side effect of aspirin.<br />
ITGB3 <strong>Gene</strong>ral Health / Clotting Factors CC TT<br />
rs2227589<br />
<strong>Gene</strong> variants associated with deep<br />
vein thrombosis.<br />
SERPINC1 <strong>Gene</strong>ral Health / Clotting Factors TT CC
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