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rs398122690

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398122690(C;G)
Make rs398122690(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position43063954
GeneBRCA1
is asnp
is mentioned by
dbSNPrs398122690
ebirs398122690
HLIrs398122690
Exacrs398122690
Varsomers398122690
Maprs398122690
PheGenIrs398122690
hapmaprs398122690
1000 genomesrs398122690
hgdprs398122690
ensemblrs398122690
gopubmedrs398122690
geneviewrs398122690
scholarrs398122690
googlers398122690
pharmgkbrs398122690
gwascentralrs398122690
openSNPrs398122690
23andMers398122690
23andMe allrs398122690
SNP Nexus

SNPshotrs398122690
SNPdbers398122690
MSV3drs398122690
GWAS Ctlgrs398122690
Max Magnitude0
ClinVar
Risk rs398122690(G;G)
Alt rs398122690(G;G)
Reference rs398122690(C;C)
Significance Probable-Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA1
CLNDBN Breast-ovarian cancer, familial 1
Reversed 1
HGVS NC_000017.10:g.41215971G>C
CLNSRC ClinVar
CLNACC RCV000077154.2,