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rs397507627

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397507627(-;-)
Make rs397507627(-;C)
ReferenceGRCh38 38.1/141
Chromosome13
Position32336797
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507627
ebirs397507627
HLIrs397507627
Exacrs397507627
Varsomers397507627
Maprs397507627
PheGenIrs397507627
hapmaprs397507627
1000 genomesrs397507627
hgdprs397507627
ensemblrs397507627
gopubmedrs397507627
geneviewrs397507627
scholarrs397507627
googlers397507627
pharmgkbrs397507627
gwascentralrs397507627
openSNPrs397507627
23andMers397507627
23andMe allrs397507627
SNP Nexus

SNPshotrs397507627
SNPdbers397507627
MSV3drs397507627
GWAS Ctlgrs397507627
Max Magnitude0
ClinVar
Risk rs397507627(;)
Alt rs397507627(;)
Reference rs397507627(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.32910934delC
CLNSRC ClinVar
CLNACC RCV000043995.2,