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rs398122744

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Make rs398122744(-;-)
Make rs398122744(-;TG)
ReferenceGRCh38 38.1/141
Chromosome13
Position32336608
GeneBRCA2
is asnp
is mentioned by
dbSNPrs398122744
ebirs398122744
HLIrs398122744
Exacrs398122744
Varsomers398122744
Maprs398122744
PheGenIrs398122744
hapmaprs398122744
1000 genomesrs398122744
hgdprs398122744
ensemblrs398122744
gopubmedrs398122744
geneviewrs398122744
scholarrs398122744
googlers398122744
pharmgkbrs398122744
gwascentralrs398122744
openSNPrs398122744
23andMers398122744
23andMe allrs398122744
SNP Nexus

SNPshotrs398122744
SNPdbers398122744
MSV3drs398122744
GWAS Ctlgrs398122744
Max Magnitude0
ClinVar
Risk rs398122744(;)
Alt rs398122744(;)
Reference rs398122744(TG;TG)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32910745_32910746delTG
CLNSRC ClinVar
CLNACC RCV000077681.2,