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rs397508880

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397508880(A;T)
Make rs397508880(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43094012
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397508880
ebirs397508880
HLIrs397508880
Exacrs397508880
Varsomers397508880
Maprs397508880
PheGenIrs397508880
hapmaprs397508880
1000 genomesrs397508880
hgdprs397508880
ensemblrs397508880
gopubmedrs397508880
geneviewrs397508880
scholarrs397508880
googlers397508880
pharmgkbrs397508880
gwascentralrs397508880
openSNPrs397508880
23andMers397508880
23andMe allrs397508880
SNP Nexus

SNPshotrs397508880
SNPdbers397508880
MSV3drs397508880
GWAS Ctlgrs397508880
Max Magnitude0
ClinVar
Risk rs397508880(T;T)
Alt rs397508880(T;T)
Reference rs397508880(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.41246029T>A
CLNSRC ClinVar
CLNACC RCV000047512.2,