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rs397507919

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397507919(-;-)
Make rs397507919(-;C)
ReferenceGRCh38 38.1/141
Chromosome13
Position32356530
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397507919
ebirs397507919
HLIrs397507919
Exacrs397507919
Varsomers397507919
Maprs397507919
PheGenIrs397507919
hapmaprs397507919
1000 genomesrs397507919
hgdprs397507919
ensemblrs397507919
gopubmedrs397507919
geneviewrs397507919
scholarrs397507919
googlers397507919
pharmgkbrs397507919
gwascentralrs397507919
openSNPrs397507919
23andMers397507919
23andMe allrs397507919
SNP Nexus

SNPshotrs397507919
SNPdbers397507919
MSV3drs397507919
GWAS Ctlgrs397507919
Max Magnitude0
ClinVar
Risk rs397507919(;)
Alt rs397507919(;)
Reference rs397507919(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.32930667delC
CLNSRC ClinVar
CLNACC RCV000045240.2,