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rs397507937

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397507937(A;T)
Make rs397507937(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32331012
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507937
ebirs397507937
HLIrs397507937
Exacrs397507937
Varsomers397507937
Maprs397507937
PheGenIrs397507937
hapmaprs397507937
1000 genomesrs397507937
hgdprs397507937
ensemblrs397507937
gopubmedrs397507937
geneviewrs397507937
scholarrs397507937
googlers397507937
pharmgkbrs397507937
gwascentralrs397507937
openSNPrs397507937
23andMers397507937
23andMe allrs397507937
SNP Nexus

SNPshotrs397507937
SNPdbers397507937
MSV3drs397507937
GWAS Ctlgrs397507937
Max Magnitude0
ClinVar
Risk rs397507937(T;T)
Alt rs397507937(T;T)
Reference rs397507937(A;A)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32905149A>T
CLNSRC ClinVar
CLNACC RCV000045304.2,