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rs397507610

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397507610(-;-)
Make rs397507610(-;A)
Make rs397507610(A;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32333329
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507610
ebirs397507610
HLIrs397507610
Exacrs397507610
Varsomers397507610
Maprs397507610
PheGenIrs397507610
hapmaprs397507610
1000 genomesrs397507610
hgdprs397507610
ensemblrs397507610
gopubmedrs397507610
geneviewrs397507610
scholarrs397507610
googlers397507610
pharmgkbrs397507610
gwascentralrs397507610
openSNPrs397507610
23andMers397507610
23andMe allrs397507610
SNP Nexus

SNPshotrs397507610
SNPdbers397507610
MSV3drs397507610
GWAS Ctlgrs397507610
Max Magnitude0
ClinVar
Risk rs397507610(A;A)
Alt rs397507610(A;A)
Reference rs397507610(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32907466dupA
CLNSRC ClinVar
CLNACC RCV000043908.2,