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rs397507774

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397507774(-;-)
Make rs397507774(-;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32339563
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507774
ebirs397507774
HLIrs397507774
Exacrs397507774
Varsomers397507774
Maprs397507774
PheGenIrs397507774
hapmaprs397507774
1000 genomesrs397507774
hgdprs397507774
ensemblrs397507774
gopubmedrs397507774
geneviewrs397507774
scholarrs397507774
googlers397507774
pharmgkbrs397507774
gwascentralrs397507774
openSNPrs397507774
23andMers397507774
23andMe allrs397507774
SNP Nexus

SNPshotrs397507774
SNPdbers397507774
MSV3drs397507774
GWAS Ctlgrs397507774
Max Magnitude0
ClinVar
Risk rs397507774(;)
Alt rs397507774(;)
Reference rs397507774(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.32913700delA
CLNSRC ClinVar
CLNACC RCV000044607.2,