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rs397507854

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397507854(-;-)
Make rs397507854(-;C)
ReferenceGRCh38 38.1/141
Chromosome13
Position32340783
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507854
ebirs397507854
HLIrs397507854
Exacrs397507854
Varsomers397507854
Maprs397507854
PheGenIrs397507854
hapmaprs397507854
1000 genomesrs397507854
hgdprs397507854
ensemblrs397507854
gopubmedrs397507854
geneviewrs397507854
scholarrs397507854
googlers397507854
pharmgkbrs397507854
gwascentralrs397507854
openSNPrs397507854
23andMers397507854
23andMe allrs397507854
SNP Nexus

SNPshotrs397507854
SNPdbers397507854
MSV3drs397507854
GWAS Ctlgrs397507854
Max Magnitude0
ClinVar
Risk rs397507854(;)
Alt rs397507854(;)
Reference rs397507854(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.32914920delC
CLNSRC ClinVar
CLNACC RCV000044943.2,