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rs397507681

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397507681(-;-)
Make rs397507681(-;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32325129
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507681
ebirs397507681
HLIrs397507681
Exacrs397507681
Varsomers397507681
Maprs397507681
PheGenIrs397507681
hapmaprs397507681
1000 genomesrs397507681
hgdprs397507681
ensemblrs397507681
gopubmedrs397507681
geneviewrs397507681
scholarrs397507681
googlers397507681
pharmgkbrs397507681
gwascentralrs397507681
openSNPrs397507681
23andMers397507681
23andMe allrs397507681
SNP Nexus

SNPshotrs397507681
SNPdbers397507681
MSV3drs397507681
GWAS Ctlgrs397507681
Max Magnitude0
ClinVar
Risk rs397507681(;)
Alt rs397507681(;)
Reference rs397507681(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.32899266delA
CLNSRC ClinVar
CLNACC RCV000044249.2,