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rs397507987

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397507987(A;A)
Make rs397507987(A;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32370521
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507987
ebirs397507987
HLIrs397507987
Exacrs397507987
Varsomers397507987
Maprs397507987
PheGenIrs397507987
hapmaprs397507987
1000 genomesrs397507987
hgdprs397507987
ensemblrs397507987
gopubmedrs397507987
geneviewrs397507987
scholarrs397507987
googlers397507987
pharmgkbrs397507987
gwascentralrs397507987
openSNPrs397507987
23andMers397507987
23andMe allrs397507987
SNP Nexus

SNPshotrs397507987
SNPdbers397507987
MSV3drs397507987
GWAS Ctlgrs397507987
Max Magnitude0
ClinVar
Risk rs397507987(A;A)
Alt rs397507987(A;A)
Reference rs397507987(T;T)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32944658T>A
CLNSRC ClinVar
CLNACC RCV000045522.2,