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rs397509326

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397509326(A;G)
Make rs397509326(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position43115781
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509326
ebirs397509326
HLIrs397509326
Exacrs397509326
Varsomers397509326
Maprs397509326
PheGenIrs397509326
hapmaprs397509326
1000 genomesrs397509326
hgdprs397509326
ensemblrs397509326
gopubmedrs397509326
geneviewrs397509326
scholarrs397509326
googlers397509326
pharmgkbrs397509326
gwascentralrs397509326
openSNPrs397509326
23andMers397509326
23andMe allrs397509326
SNP Nexus

SNPshotrs397509326
SNPdbers397509326
MSV3drs397509326
GWAS Ctlgrs397509326
Max Magnitude0
ClinVar
Risk rs397509326(C,G;C,G)
Alt rs397509326(C,G;C,G)
Reference rs397509326(A;A)
Significance Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer Hereditary breast and ovarian cancer syndrome
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 1 Hereditary breast and ovarian cancer syndrome
Reversed 1
HGVS NC_000017.10:g.41267798T>C; NC_000017.10:g.41267798T>G
CLNSRC ClinVar
CLNACC RCV000049149.2, RCV000238783.1, RCV000123286.1,