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rs397507706

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397507706(-;-)
Make rs397507706(-;A)
Make rs397507706(A;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32338456
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507706
ebirs397507706
HLIrs397507706
Exacrs397507706
Varsomers397507706
Maprs397507706
PheGenIrs397507706
hapmaprs397507706
1000 genomesrs397507706
hgdprs397507706
ensemblrs397507706
gopubmedrs397507706
geneviewrs397507706
scholarrs397507706
googlers397507706
pharmgkbrs397507706
gwascentralrs397507706
openSNPrs397507706
23andMers397507706
23andMe allrs397507706
SNP Nexus

SNPshotrs397507706
SNPdbers397507706
MSV3drs397507706
GWAS Ctlgrs397507706
Max Magnitude0
ClinVar
Risk rs397507706(A;A)
Alt rs397507706(A;A)
Reference rs397507706(;)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32912593dupA
CLNSRC ClinVar
CLNACC RCV000044351.2,