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rs397507772

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397507772(-;-)
Make rs397507772(-;A)
Make rs397507772(A;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32316511
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507772
ebirs397507772
HLIrs397507772
Exacrs397507772
Varsomers397507772
Maprs397507772
PheGenIrs397507772
hapmaprs397507772
1000 genomesrs397507772
hgdprs397507772
ensemblrs397507772
gopubmedrs397507772
geneviewrs397507772
scholarrs397507772
googlers397507772
pharmgkbrs397507772
gwascentralrs397507772
openSNPrs397507772
23andMers397507772
23andMe allrs397507772
SNP Nexus

SNPshotrs397507772
SNPdbers397507772
MSV3drs397507772
GWAS Ctlgrs397507772
Max Magnitude0
ClinVar
Risk rs397507772(A;A)
Alt rs397507772(A;A)
Reference rs397507772(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32890648dupA
CLNSRC ClinVar
CLNACC RCV000044605.2,