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rs398122622

From SNPedia

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


Make rs398122622(-;-)
ReferenceGRCh38 38.1/141
Chromosome13
Position32398321
GeneBRCA2
is asnp
is mentioned by
dbSNPrs398122622
dbSNP (old)rs398122622
ClinGenrs398122622
ebirs398122622
HLIrs398122622
Exacrs398122622
Gnomadrs398122622
Varsomers398122622
Maprs398122622
PheGenIrs398122622
Biobankrs398122622
1000 genomesrs398122622
hgdprs398122622
ensemblrs398122622
gopubmedrs398122622
geneviewrs398122622
scholarrs398122622
googlers398122622
pharmgkbrs398122622
gwascentralrs398122622
openSNPrs398122622
23andMers398122622
23andMe allrs398122622
SNP Nexus

SNPshotrs398122622
SNPdbers398122622
MSV3drs398122622
GWAS Ctlgrs398122622
Max Magnitude6
ClinVar
Risk rs398122622(-;-)
Alt rs398122622(-;-)
Reference Rs398122622(G;G)
Significance Pathogenic
Disease Breast-ovarian cancer Hereditary breast and ovarian cancer syndrome Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 Hereditary breast and ovarian cancer syndrome Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32972458delG
CLNSRC ClinVar
CLNACC RCV000077051.4, RCV000197732.1, RCV000217558.1,