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rs397507752

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397507752(-;-)
Make rs397507752(-;C)
ReferenceGRCh38 38.1/141
Chromosome13
Position32339307
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507752
ebirs397507752
HLIrs397507752
Exacrs397507752
Varsomers397507752
Maprs397507752
PheGenIrs397507752
hapmaprs397507752
1000 genomesrs397507752
hgdprs397507752
ensemblrs397507752
gopubmedrs397507752
geneviewrs397507752
scholarrs397507752
googlers397507752
pharmgkbrs397507752
gwascentralrs397507752
openSNPrs397507752
23andMers397507752
23andMe allrs397507752
SNP Nexus

SNPshotrs397507752
SNPdbers397507752
MSV3drs397507752
GWAS Ctlgrs397507752
Max Magnitude0
ClinVar
Risk rs397507752(;)
Alt rs397507752(;)
Reference rs397507752(C;C)
Significance Untested
Disease Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32913444delC
CLNSRC ClinVar
CLNACC RCV000044530.2,