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rs398122775

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TT;TT) 0 common in clinvar
Make rs398122775(-;-)
Make rs398122775(-;TT)
ReferenceGRCh38 38.1/141
Chromosome13
Position32338355
GeneBRCA2
is asnp
is mentioned by
dbSNPrs398122775
ebirs398122775
HLIrs398122775
Exacrs398122775
Varsomers398122775
Maprs398122775
PheGenIrs398122775
hapmaprs398122775
1000 genomesrs398122775
hgdprs398122775
ensemblrs398122775
gopubmedrs398122775
geneviewrs398122775
scholarrs398122775
googlers398122775
pharmgkbrs398122775
gwascentralrs398122775
openSNPrs398122775
23andMers398122775
23andMe allrs398122775
SNP Nexus

SNPshotrs398122775
SNPdbers398122775
MSV3drs398122775
GWAS Ctlgrs398122775
Max Magnitude0
ClinVar
Risk rs398122775(;)
Alt rs398122775(;)
Reference rs398122775(TT;TT)
Significance Pathogenic
Disease Breast-ovarian cancer Familial cancer of breast
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 Familial cancer of breast
Reversed 0
HGVS NC_000013.10:g.32912492_32912493delTT
CLNSRC ClinVar
CLNACC RCV000077720.2, RCV000160282.1,