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rs397508940

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397508940(A;C)
Make rs397508940(C;C)
ReferenceGRCh38 38.1/141
Chromosome17
Position43104958
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397508940
ebirs397508940
HLIrs397508940
Exacrs397508940
Varsomers397508940
Maprs397508940
PheGenIrs397508940
hapmaprs397508940
1000 genomesrs397508940
hgdprs397508940
ensemblrs397508940
gopubmedrs397508940
geneviewrs397508940
scholarrs397508940
googlers397508940
pharmgkbrs397508940
gwascentralrs397508940
openSNPrs397508940
23andMers397508940
23andMe allrs397508940
SNP Nexus

SNPshotrs397508940
SNPdbers397508940
MSV3drs397508940
GWAS Ctlgrs397508940
Max Magnitude0
ClinVar
Risk rs397508940(C;C)
Alt rs397508940(C;C)
Reference rs397508940(A;A)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA1
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000017.10:g.41256975T>G
CLNSRC ClinVar
CLNACC RCV000047728.2,