rs374435098
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs374435098(C;T) |
Make rs374435098(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 17 |
Position | 43079400 |
Gene | BRCA1 |
is a | snp |
is | mentioned by |
dbSNP | rs374435098 |
dbSNP (classic) | rs374435098 |
ClinGen | rs374435098 |
ebi | rs374435098 |
HLI | rs374435098 |
Exac | rs374435098 |
Gnomad | rs374435098 |
Varsome | rs374435098 |
LitVar | rs374435098 |
Map | rs374435098 |
PheGenI | rs374435098 |
Biobank | rs374435098 |
1000 genomes | rs374435098 |
hgdp | rs374435098 |
ensembl | rs374435098 |
geneview | rs374435098 |
scholar | rs374435098 |
rs374435098 | |
pharmgkb | rs374435098 |
gwascentral | rs374435098 |
openSNP | rs374435098 |
23andMe | rs374435098 |
SNPshot | rs374435098 |
SNPdbe | rs374435098 |
MSV3d | rs374435098 |
GWAS Ctlg | rs374435098 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs374435098(T;T) |
Alt | rs374435098(T;T) |
Reference | Rs374435098(C;C) |
Significance | Probable-Pathogenic |
Disease | Hereditary breast and ovarian cancer syndrome |
Variation | info |
Gene | BRCA1 |
CLNDBN | Hereditary breast and ovarian cancer syndrome |
Reversed | 0 |
HGVS | NC_000017.10:g.41231417C>T |
CLNSRC | |
CLNACC | RCV000149888.2, |