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rs398122783

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398122783(-;-)
Make rs398122783(-;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position32338907
GeneBRCA2
is asnp
is mentioned by
dbSNPrs398122783
ebirs398122783
HLIrs398122783
Exacrs398122783
Varsomers398122783
Maprs398122783
PheGenIrs398122783
hapmaprs398122783
1000 genomesrs398122783
hgdprs398122783
ensemblrs398122783
gopubmedrs398122783
geneviewrs398122783
scholarrs398122783
googlers398122783
pharmgkbrs398122783
gwascentralrs398122783
openSNPrs398122783
23andMers398122783
23andMe allrs398122783
SNP Nexus

SNPshotrs398122783
SNPdbers398122783
MSV3drs398122783
GWAS Ctlgrs398122783
Max Magnitude0
ClinVar
Risk rs398122783(;)
Alt rs398122783(;)
Reference rs398122783(G;G)
Significance Pathogenic
Disease Breast-ovarian cancer Hereditary cancer-predisposing syndrome Hereditary breast and ovarian cancer syndrome
Variation info
Gene BRCA2
CLNDBN Breast-ovarian cancer, familial 2 Hereditary cancer-predisposing syndrome Hereditary breast and ovarian cancer syndrome
Reversed 0
HGVS NC_000013.10:g.32913044delG
CLNSRC Ambry Genetics ClinVar
CLNACC RCV000077730.3, RCV000129446.2, RCV000204632.2,