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rs398122601

From SNPedia

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


Make rs398122601(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32363510
GeneBRCA2
is asnp
is mentioned by
dbSNPrs398122601
dbSNP (classic)rs398122601
ClinGenrs398122601
ebirs398122601
HLIrs398122601
Exacrs398122601
Gnomadrs398122601
Varsomers398122601
LitVarrs398122601
Maprs398122601
PheGenIrs398122601
Biobankrs398122601
1000 genomesrs398122601
hgdprs398122601
ensemblrs398122601
geneviewrs398122601
scholarrs398122601
googlers398122601
pharmgkbrs398122601
gwascentralrs398122601
openSNPrs398122601
23andMers398122601
SNPshotrs398122601
SNPdbers398122601
MSV3drs398122601
GWAS Ctlgrs398122601
Max Magnitude6
ClinVar
Risk rs398122601(-;-)
Alt rs398122601(-;-)
Reference Rs398122601(G;G)
Significance Pathogenic
Disease Breast-ovarian cancer Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32937647delG
CLNSRC ClinVar
CLNACC RCV000077023.3, RCV000216064.1,