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rs397507991

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397507991(-;-)
Make rs397507991(-;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32371014
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507991
ebirs397507991
HLIrs397507991
Exacrs397507991
Varsomers397507991
Maprs397507991
PheGenIrs397507991
hapmaprs397507991
1000 genomesrs397507991
hgdprs397507991
ensemblrs397507991
gopubmedrs397507991
geneviewrs397507991
scholarrs397507991
googlers397507991
pharmgkbrs397507991
gwascentralrs397507991
openSNPrs397507991
23andMers397507991
23andMe allrs397507991
SNP Nexus

SNPshotrs397507991
SNPdbers397507991
MSV3drs397507991
GWAS Ctlgrs397507991
Max Magnitude0
ClinVar
Risk rs397507991(;)
Alt rs397507991(;)
Reference rs397507991(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.32945151delA
CLNSRC ClinVar
CLNACC RCV000045553.2,