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rs397507990

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AA;AA) 0 common in clinvar
Make rs397507990(-;-)
Make rs397507990(-;AA)
ReferenceGRCh38 38.1/141
Chromosome13
Position32371000
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507990
ebirs397507990
HLIrs397507990
Exacrs397507990
Varsomers397507990
Maprs397507990
PheGenIrs397507990
hapmaprs397507990
1000 genomesrs397507990
hgdprs397507990
ensemblrs397507990
gopubmedrs397507990
geneviewrs397507990
scholarrs397507990
googlers397507990
pharmgkbrs397507990
gwascentralrs397507990
openSNPrs397507990
23andMers397507990
23andMe allrs397507990
SNP Nexus

SNPshotrs397507990
SNPdbers397507990
MSV3drs397507990
GWAS Ctlgrs397507990
Max Magnitude0
ClinVar
Risk rs397507990(;)
Alt rs397507990(;)
Reference rs397507990(AA;AA)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32945137_32945138delAA
CLNSRC ClinVar
CLNACC RCV000045548.2,