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rs397509342

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397509342(-;-)
Make rs397509342(-;A)
ReferenceGRCh38 38.1/141
Chromosome13
Position32337190
GeneBRCA2
is asnp
is mentioned by
dbSNPrs397509342
ebirs397509342
HLIrs397509342
Exacrs397509342
Varsomers397509342
Maprs397509342
PheGenIrs397509342
hapmaprs397509342
1000 genomesrs397509342
hgdprs397509342
ensemblrs397509342
gopubmedrs397509342
geneviewrs397509342
scholarrs397509342
googlers397509342
pharmgkbrs397509342
gwascentralrs397509342
openSNPrs397509342
23andMers397509342
23andMe allrs397509342
SNP Nexus

SNPshotrs397509342
SNPdbers397509342
MSV3drs397509342
GWAS Ctlgrs397509342
Max Magnitude0
ClinVar
Risk rs397509342(;)
Alt rs397509342(;)
Reference rs397509342(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.32911327delA
CLNSRC ClinVar
CLNACC RCV000049221.2,