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rs397509295

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397509295(A;A)
Make rs397509295(A;C)
ReferenceGRCh38 38.1/141
Chromosome17
Position43045729
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509295
ebirs397509295
HLIrs397509295
Exacrs397509295
Varsomers397509295
Maprs397509295
PheGenIrs397509295
hapmaprs397509295
1000 genomesrs397509295
hgdprs397509295
ensemblrs397509295
gopubmedrs397509295
geneviewrs397509295
scholarrs397509295
googlers397509295
pharmgkbrs397509295
gwascentralrs397509295
openSNPrs397509295
23andMers397509295
23andMe allrs397509295
SNP Nexus

SNPshotrs397509295
SNPdbers397509295
MSV3drs397509295
GWAS Ctlgrs397509295
Max Magnitude0
ClinVar
Risk rs397509295(A,G;A,G)
Alt rs397509295(A,G;A,G)
Reference rs397509295(C;C)
Significance Pathogenic
Disease Familial cancer of breast Breast-ovarian cancer
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast Breast-ovarian cancer, familial 1
Reversed 1
HGVS NC_000017.10:g.41197746G>T
CLNSRC ClinVar
CLNACC RCV000049044.2, RCV000083222.2,