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rs398122635

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398122635(A;A)
Make rs398122635(A;C)
ReferenceGRCh38 38.1/141
Chromosome17
Position43106527
GeneBRCA1
is asnp
is mentioned by
dbSNPrs398122635
ebirs398122635
HLIrs398122635
Exacrs398122635
Varsomers398122635
Maprs398122635
PheGenIrs398122635
hapmaprs398122635
1000 genomesrs398122635
hgdprs398122635
ensemblrs398122635
gopubmedrs398122635
geneviewrs398122635
scholarrs398122635
googlers398122635
pharmgkbrs398122635
gwascentralrs398122635
openSNPrs398122635
23andMers398122635
23andMe allrs398122635
SNP Nexus

SNPshotrs398122635
SNPdbers398122635
MSV3drs398122635
GWAS Ctlgrs398122635
Max Magnitude0
ClinVar
Risk rs398122635(A,T;A,T)
Alt rs398122635(A,T;A,T)
Reference rs398122635(C;C)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA1
CLNDBN Breast-ovarian cancer, familial 1
Reversed 1
HGVS NC_000017.10:g.41258544G>T
CLNSRC ClinVar
CLNACC RCV000077070.2,