Have questions? Visit https://www.reddit.com/r/SNPedia

rs397507219

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397507219(C;C)
Make rs397507219(C;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43091749
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397507219
ebirs397507219
HLIrs397507219
Exacrs397507219
Varsomers397507219
Maprs397507219
PheGenIrs397507219
hapmaprs397507219
1000 genomesrs397507219
hgdprs397507219
ensemblrs397507219
gopubmedrs397507219
geneviewrs397507219
scholarrs397507219
googlers397507219
pharmgkbrs397507219
gwascentralrs397507219
openSNPrs397507219
23andMers397507219
23andMe allrs397507219
SNP Nexus

SNPshotrs397507219
SNPdbers397507219
MSV3drs397507219
GWAS Ctlgrs397507219
Max Magnitude0
ClinVar
Risk rs397507219(C,G;C,G)
Alt rs397507219(C,G;C,G)
Reference rs397507219(T;T)
Significance Untested
Disease Familial cancer of breast Breast-ovarian cancer Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 1 Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.41243766A>C; NC_000017.10:g.41243766A>G
CLNSRC ClinVar Ambry Genetics
CLNACC RCV000048330.2, RCV000031129.3, RCV000129886.2,