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rs397507868

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397507868(-;-)
Make rs397507868(-;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32340944
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507868
ebirs397507868
HLIrs397507868
Exacrs397507868
Varsomers397507868
Maprs397507868
PheGenIrs397507868
hapmaprs397507868
1000 genomesrs397507868
hgdprs397507868
ensemblrs397507868
gopubmedrs397507868
geneviewrs397507868
scholarrs397507868
googlers397507868
pharmgkbrs397507868
gwascentralrs397507868
openSNPrs397507868
23andMers397507868
23andMe allrs397507868
SNP Nexus

SNPshotrs397507868
SNPdbers397507868
MSV3drs397507868
GWAS Ctlgrs397507868
Max Magnitude0
ClinVar
Risk rs397507868(;)
Alt rs397507868(;)
Reference rs397507868(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.32915081delA
CLNSRC ClinVar
CLNACC RCV000044987.2,