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rs200432771

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;C) 6 BRCA1 variant considered pathogenic for breast cancer
(C;C) 0 common in clinvar
Make rs200432771(C;T)
Make rs200432771(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43071011
GeneBRCA1
is asnp
is mentioned by
dbSNPrs200432771
dbSNP (old)rs200432771
ClinGenrs200432771
ebirs200432771
HLIrs200432771
Exacrs200432771
Gnomadrs200432771
Varsomers200432771
Maprs200432771
PheGenIrs200432771
Biobankrs200432771
1000 genomesrs200432771
hgdprs200432771
ensemblrs200432771
gopubmedrs200432771
geneviewrs200432771
scholarrs200432771
googlers200432771
pharmgkbrs200432771
gwascentralrs200432771
openSNPrs200432771
23andMers200432771
23andMe allrs200432771
SNP Nexus

SNPshotrs200432771
SNPdbers200432771
MSV3drs200432771
GWAS Ctlgrs200432771
Max Magnitude6
ClinVar
Risk rs200432771(A;A) rs200432771(T;T)
Alt rs200432771(A;A) rs200432771(T;T)
Reference Rs200432771(C;C)
Significance Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer Hereditary cancer-predisposing syndrome not provided
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 1 Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000017.10:g.41223028C>A; NC_000017.10:g.41223028C>T
CLNSRC Breast Cancer Information Core (BRCA1)
CLNACC RCV000048688.2, RCV000112420.3, RCV000129569.2, RCV000034755.1, RCV000410023.1,