rs118203905
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
(A;G) | 3 | Carrier of a Factor V deficiency mutation |
(G;G) | 5.5 | Hemophilia A (severity varies) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 169555300 |
Gene | F5 |
is a | snp |
is | mentioned by |
dbSNP | rs118203905 |
dbSNP (classic) | rs118203905 |
ClinGen | rs118203905 |
ebi | rs118203905 |
HLI | rs118203905 |
Exac | rs118203905 |
Gnomad | rs118203905 |
Varsome | rs118203905 |
LitVar | rs118203905 |
Map | rs118203905 |
PheGenI | rs118203905 |
Biobank | rs118203905 |
1000 genomes | rs118203905 |
hgdp | rs118203905 |
ensembl | rs118203905 |
geneview | rs118203905 |
scholar | rs118203905 |
rs118203905 | |
pharmgkb | rs118203905 |
gwascentral | rs118203905 |
openSNP | rs118203905 |
23andMe | rs118203905 |
SNPshot | rs118203905 |
SNPdbe | rs118203905 |
MSV3d | rs118203905 |
GWAS Ctlg | rs118203905 |
GMAF | 0.001377 |
Max Magnitude | 5.5 |
ClinVar | |
---|---|
Risk | Rs118203905(G;G) |
Alt | Rs118203905(G;G) |
Reference | Rs118203905(A;A) |
Significance | Pathogenic |
Disease | Factor V Hong Kong |
Variation | info |
Gene | F5 |
CLNDBN | Factor V Hong Kong |
Reversed | 1 |
HGVS | NC_000001.10:g.169524538T>C |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000000677.2, |