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rs398122786

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;T) 6 BRCA2 variant considered pathogenic for breast cancer
(T;T) 0 common in clinvar


Make rs398122786(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32339202
GeneBRCA2
is asnp
is mentioned by
dbSNPrs398122786
ClinGenrs398122786
ebirs398122786
HLIrs398122786
Exacrs398122786
Varsomers398122786
Maprs398122786
PheGenIrs398122786
hapmaprs398122786
1000 genomesrs398122786
hgdprs398122786
ensemblrs398122786
gopubmedrs398122786
geneviewrs398122786
scholarrs398122786
googlers398122786
pharmgkbrs398122786
gwascentralrs398122786
openSNPrs398122786
23andMers398122786
23andMe allrs398122786
SNP Nexus

SNPshotrs398122786
SNPdbers398122786
MSV3drs398122786
GWAS Ctlgrs398122786
Max Magnitude6
ClinVar
Risk rs398122786(G;G)
Alt rs398122786(G;G)
Reference Rs398122786(T;T)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2
Reversed 0
HGVS NC_000013.10:g.32913339T>G
CLNSRC ClinVar
CLNACC RCV000077734.3,