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rs397509211

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397509211(G;T)
Make rs397509211(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43070923
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397509211
ebirs397509211
HLIrs397509211
Exacrs397509211
Varsomers397509211
Maprs397509211
PheGenIrs397509211
hapmaprs397509211
1000 genomesrs397509211
hgdprs397509211
ensemblrs397509211
gopubmedrs397509211
geneviewrs397509211
scholarrs397509211
googlers397509211
pharmgkbrs397509211
gwascentralrs397509211
openSNPrs397509211
23andMers397509211
23andMe allrs397509211
SNP Nexus

SNPshotrs397509211
SNPdbers397509211
MSV3drs397509211
GWAS Ctlgrs397509211
Max Magnitude0
ClinVar
Risk rs397509211(A,T;A,T)
Alt rs397509211(A,T;A,T)
Reference rs397509211(G;G)
Significance Other
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.41222940C>A; NC_000017.10:g.41222940C>T
CLNSRC Breast Cancer Information Core (BRCA1)
CLNACC RCV000048723.2, RCV000083057.4, RCV000197490.1,