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rs397507601

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397507601(-;-)
Make rs397507601(-;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32333150
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507601
ebirs397507601
HLIrs397507601
Exacrs397507601
Varsomers397507601
Maprs397507601
PheGenIrs397507601
hapmaprs397507601
1000 genomesrs397507601
hgdprs397507601
ensemblrs397507601
gopubmedrs397507601
geneviewrs397507601
scholarrs397507601
googlers397507601
pharmgkbrs397507601
gwascentralrs397507601
openSNPrs397507601
23andMers397507601
23andMe allrs397507601
SNP Nexus

SNPshotrs397507601
SNPdbers397507601
MSV3drs397507601
GWAS Ctlgrs397507601
Max Magnitude0
ClinVar
Risk rs397507601(;)
Alt rs397507601(;)
Reference rs397507601(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.32907287delA
CLNSRC ClinVar
CLNACC RCV000043859.2,