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rs397507694

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AA;AA) 0 common in clinvar
Make rs397507694(-;-)
Make rs397507694(-;AA)
ReferenceGRCh38 38.1/141
Chromosome13
Position32338221
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507694
ebirs397507694
HLIrs397507694
Exacrs397507694
Varsomers397507694
Maprs397507694
PheGenIrs397507694
hapmaprs397507694
1000 genomesrs397507694
hgdprs397507694
ensemblrs397507694
gopubmedrs397507694
geneviewrs397507694
scholarrs397507694
googlers397507694
pharmgkbrs397507694
gwascentralrs397507694
openSNPrs397507694
23andMers397507694
23andMe allrs397507694
SNP Nexus

SNPshotrs397507694
SNPdbers397507694
MSV3drs397507694
GWAS Ctlgrs397507694
Max Magnitude0
ClinVar
Risk rs397507694(;)
Alt rs397507694(;)
Reference rs397507694(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.32912358_32912359delAA
CLNSRC ClinVar
CLNACC RCV000044293.2,