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rs397507680

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397507680(-;-)
Make rs397507680(-;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32325123
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507680
ebirs397507680
HLIrs397507680
Exacrs397507680
Varsomers397507680
Maprs397507680
PheGenIrs397507680
hapmaprs397507680
1000 genomesrs397507680
hgdprs397507680
ensemblrs397507680
gopubmedrs397507680
geneviewrs397507680
scholarrs397507680
googlers397507680
pharmgkbrs397507680
gwascentralrs397507680
openSNPrs397507680
23andMers397507680
23andMe allrs397507680
SNP Nexus

SNPshotrs397507680
SNPdbers397507680
MSV3drs397507680
GWAS Ctlgrs397507680
Max Magnitude0
ClinVar
Risk rs397507680(;)
Alt rs397507680(;)
Reference rs397507680(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.32899260delA
CLNSRC ClinVar
CLNACC RCV000044236.2,