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rs397507740

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397507740(-;-)
Make rs397507740(-;A)
Make rs397507740(A;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32339084
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507740
ebirs397507740
HLIrs397507740
Exacrs397507740
Varsomers397507740
Maprs397507740
PheGenIrs397507740
hapmaprs397507740
1000 genomesrs397507740
hgdprs397507740
ensemblrs397507740
gopubmedrs397507740
geneviewrs397507740
scholarrs397507740
googlers397507740
pharmgkbrs397507740
gwascentralrs397507740
openSNPrs397507740
23andMers397507740
23andMe allrs397507740
SNP Nexus

SNPshotrs397507740
SNPdbers397507740
MSV3drs397507740
GWAS Ctlgrs397507740
Max Magnitude0
ClinVar
Risk rs397507740(A;A)
Alt rs397507740(A;A)
Reference rs397507740(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32913222dupA
CLNSRC ClinVar
CLNACC RCV000044477.2,