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rs398122539

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398122539(-;-)
Make rs398122539(-;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32340047
GeneBRCA2
is asnp
is mentioned by
dbSNPrs398122539
ebirs398122539
HLIrs398122539
Exacrs398122539
Varsomers398122539
Maprs398122539
PheGenIrs398122539
hapmaprs398122539
1000 genomesrs398122539
hgdprs398122539
ensemblrs398122539
gopubmedrs398122539
geneviewrs398122539
scholarrs398122539
googlers398122539
pharmgkbrs398122539
gwascentralrs398122539
openSNPrs398122539
23andMers398122539
23andMe allrs398122539
SNP Nexus

SNPshotrs398122539
SNPdbers398122539
MSV3drs398122539
GWAS Ctlgrs398122539
Max Magnitude0
ClinVar
Risk rs398122539(;)
Alt rs398122539(;)
Reference rs398122539(G;G)
Significance Pathogenic
Disease Breast-ovarian cancer not provided
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 not provided
Reversed 0
HGVS NC_000013.10:g.32914184delG
CLNSRC ClinVar
CLNACC RCV000076940.2, RCV000235464.1,