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rs397507712

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397507712(-;-)
Make rs397507712(-;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32338578
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507712
ebirs397507712
HLIrs397507712
Exacrs397507712
Varsomers397507712
Maprs397507712
PheGenIrs397507712
hapmaprs397507712
1000 genomesrs397507712
hgdprs397507712
ensemblrs397507712
gopubmedrs397507712
geneviewrs397507712
scholarrs397507712
googlers397507712
pharmgkbrs397507712
gwascentralrs397507712
openSNPrs397507712
23andMers397507712
23andMe allrs397507712
SNP Nexus

SNPshotrs397507712
SNPdbers397507712
MSV3drs397507712
GWAS Ctlgrs397507712
Max Magnitude0
ClinVar
Risk rs397507712(;)
Alt rs397507712(;)
Reference rs397507712(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.32912715delA
CLNSRC ClinVar
CLNACC RCV000044374.2,