Gene Variant Report issued

Lifestyle Genomics Research Centre Ltd.
Plymouth Science Park, 1 Davy Road, Derriford, Plymouth, PL6 8BX , UNITED KINGDOM contact us
SAMPLE PROCESSED BY:
METHOD:
DATA CHECKED FOR ACCURACY BY:
Genome Centre at BARTS and The London School of Medicine and Dentistry
Fluidigm TaqMan probe-based SNP genotyping / Illumina MiSeq, Next Generation
sequencing
Genome Centre at BARTS and The London School of Medicine and Dentistry
NOTES:
genotype has no risk alleles
genotype has one risk allele
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genotype has two risk allels
either allele can be a risk or be
beneficial
Ctr+F to activate Search Engine: Look up genes, rsids, pathways / traits
SNP RSID INTERPRET ☞ PARENT GENE & VARIANT ⚛ CATEGORY ☤ / PATHWAY ⥹ RISK ALLELES !! cp00035774
rs3211719
rs6025
rs6048
This gene encodes a protein called
coagulation factor X that helps
blood clot after an injury. Mutations
can cause deficiency of the protein,
which leads to excessive bleeding.
he F5 gene encodes a protein that is
called coagulation factor V. They
that form blood clots to stop
bleeding and trigger blood vessel
repair after an injury. Mutations can
cause abnormal bleeding.
This gene encodes a protein called
coagulation factor IX, which helps
form blood clots. Mutations can
cause blood clots to be unable to
form and lead to excessive bleeding
(hemophilia) or warfarin sensitivity,
which can cause severe bleeding
problems.
F10 General Health / Clotting Factors GG AA
F5 General Health / Clotting Factors TT CC
F9 General Health / Clotting Factors GG GG