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rs398122558

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398122558(C;G)
Make rs398122558(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position32340830
GeneBRCA2
is asnp
is mentioned by
dbSNPrs398122558
ebirs398122558
HLIrs398122558
Exacrs398122558
Varsomers398122558
Maprs398122558
PheGenIrs398122558
hapmaprs398122558
1000 genomesrs398122558
hgdprs398122558
ensemblrs398122558
gopubmedrs398122558
geneviewrs398122558
scholarrs398122558
googlers398122558
pharmgkbrs398122558
gwascentralrs398122558
openSNPrs398122558
23andMers398122558
23andMe allrs398122558
SNP Nexus

SNPshotrs398122558
SNPdbers398122558
MSV3drs398122558
GWAS Ctlgrs398122558
Max Magnitude0
ClinVar
Risk rs398122558(G,T;G,T)
Alt rs398122558(G,T;G,T)
Reference rs398122558(C;C)
Significance Pathogenic
Disease Breast-ovarian cancer not specified Hereditary cancer-predisposing syndrome Hereditary breast and ovarian cancer syndrome
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 not specified Hereditary cancer-predisposing syndrome Hereditary breast and ovarian cancer syndrome
Reversed 0
HGVS NC_000013.10:g.32914967C>G; NC_000013.10:g.32914967C>T
CLNSRC
CLNACC RCV000076967.2, RCV000160111.2, RCV000166819.1, RCV000196558.1, RCV000166433.1, RCV000225554.1,