rs149364097
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
(C;G) | 6 | Ovarian cancer susceptibility |
Make rs149364097(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 17 |
Position | 61801348 |
Gene | BRIP1 |
is a | snp |
is | mentioned by |
dbSNP | rs149364097 |
dbSNP (classic) | rs149364097 |
ClinGen | rs149364097 |
ebi | rs149364097 |
HLI | rs149364097 |
Exac | rs149364097 |
Gnomad | rs149364097 |
Varsome | rs149364097 |
LitVar | rs149364097 |
Map | rs149364097 |
PheGenI | rs149364097 |
Biobank | rs149364097 |
1000 genomes | rs149364097 |
hgdp | rs149364097 |
ensembl | rs149364097 |
geneview | rs149364097 |
scholar | rs149364097 |
rs149364097 | |
pharmgkb | rs149364097 |
gwascentral | rs149364097 |
openSNP | rs149364097 |
23andMe | rs149364097 |
SNPshot | rs149364097 |
SNPdbe | rs149364097 |
MSV3d | rs149364097 |
GWAS Ctlg | rs149364097 |
Max Magnitude | 6 |
ClinVar | |
---|---|
Risk | rs149364097(A;A) rs149364097(G;G) rs149364097(T;T) |
Alt | rs149364097(A;A) rs149364097(G;G) rs149364097(T;T) |
Reference | Rs149364097(C;C) |
Significance | Pathogenic |
Disease | Hereditary cancer-predisposing syndrome Fanconi anemia not specified not provided Familial cancer of breast |
Variation | info |
Gene | BRIP1 |
CLNDBN | Hereditary cancer-predisposing syndrome Fanconi anemia, complementation group J not specified not provided Familial cancer of breast |
Reversed | 0 |
HGVS | NC_000017.10:g.59878709C>A; NC_000017.10:g.59878709C>G; NC_000017.10:g.59878709C>T |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000213526.1, RCV000023492.2, RCV000120412.1, RCV000131544.3, RCV000216316.2, RCV000466014.1, RCV000431413.1, |