rs121964948
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs121964948(A;T) |
Make rs121964948(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 13 |
Position | 113147490 |
Gene | F10 |
is a | snp |
is | mentioned by |
dbSNP | rs121964948 |
dbSNP (classic) | rs121964948 |
ClinGen | rs121964948 |
ebi | rs121964948 |
HLI | rs121964948 |
Exac | rs121964948 |
Gnomad | rs121964948 |
Varsome | rs121964948 |
LitVar | rs121964948 |
Map | rs121964948 |
PheGenI | rs121964948 |
Biobank | rs121964948 |
1000 genomes | rs121964948 |
hgdp | rs121964948 |
ensembl | rs121964948 |
geneview | rs121964948 |
scholar | rs121964948 |
rs121964948 | |
pharmgkb | rs121964948 |
gwascentral | rs121964948 |
openSNP | rs121964948 |
23andMe | rs121964948 |
SNPshot | rs121964948 |
SNPdbe | rs121964948 |
MSV3d | rs121964948 |
GWAS Ctlg | rs121964948 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs121964948(T;T) |
Alt | rs121964948(T;T) |
Reference | Rs121964948(A;A) |
Significance | Pathogenic |
Disease | Factor X deficiency |
Variation | info |
Gene | F10 |
CLNDBN | Factor X deficiency |
Reversed | 0 |
HGVS | NC_000013.10:g.113801804A>T |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000012839.3, |