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rs397508898

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397508898(A;T)
Make rs397508898(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43106500
GeneBRCA1
is asnp
is mentioned by
dbSNPrs397508898
ebirs397508898
HLIrs397508898
Exacrs397508898
Varsomers397508898
Maprs397508898
PheGenIrs397508898
hapmaprs397508898
1000 genomesrs397508898
hgdprs397508898
ensemblrs397508898
gopubmedrs397508898
geneviewrs397508898
scholarrs397508898
googlers397508898
pharmgkbrs397508898
gwascentralrs397508898
openSNPrs397508898
23andMers397508898
23andMe allrs397508898
SNP Nexus

SNPshotrs397508898
SNPdbers397508898
MSV3drs397508898
GWAS Ctlgrs397508898
Max Magnitude0
ClinVar
Risk rs397508898(T;T)
Alt rs397508898(T;T)
Reference rs397508898(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.41258517T>A
CLNSRC ClinVar
CLNACC RCV000047560.2,