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rs397507837

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397507837(-;-)
Make rs397507837(-;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32340631
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507837
ebirs397507837
HLIrs397507837
Exacrs397507837
Varsomers397507837
Maprs397507837
PheGenIrs397507837
hapmaprs397507837
1000 genomesrs397507837
hgdprs397507837
ensemblrs397507837
gopubmedrs397507837
geneviewrs397507837
scholarrs397507837
googlers397507837
pharmgkbrs397507837
gwascentralrs397507837
openSNPrs397507837
23andMers397507837
23andMe allrs397507837
SNP Nexus

SNPshotrs397507837
SNPdbers397507837
MSV3drs397507837
GWAS Ctlgrs397507837
Max Magnitude0
ClinVar
Risk rs397507837(;)
Alt rs397507837(;)
Reference rs397507837(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.32914768delT
CLNSRC ClinVar
CLNACC RCV000044885.2,