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rs398122749

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs398122749(-;-)
Make rs398122749(-;T)
Make rs398122749(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position32336973
GeneBRCA2
is asnp
is mentioned by
dbSNPrs398122749
ebirs398122749
HLIrs398122749
Exacrs398122749
Varsomers398122749
Maprs398122749
PheGenIrs398122749
hapmaprs398122749
1000 genomesrs398122749
hgdprs398122749
ensemblrs398122749
gopubmedrs398122749
geneviewrs398122749
scholarrs398122749
googlers398122749
pharmgkbrs398122749
gwascentralrs398122749
openSNPrs398122749
23andMers398122749
23andMe allrs398122749
SNP Nexus

SNPshotrs398122749
SNPdbers398122749
MSV3drs398122749
GWAS Ctlgrs398122749
Max Magnitude0
ClinVar
Risk rs398122749(T;T)
Alt rs398122749(T;T)
Reference rs398122749(;)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32911110dupT
CLNSRC ClinVar
CLNACC RCV000077688.2,