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rs398122663

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs398122663(-;-)
Make rs398122663(-;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43092877
GeneBRCA1
is asnp
is mentioned by
dbSNPrs398122663
ebirs398122663
HLIrs398122663
Exacrs398122663
Varsomers398122663
Maprs398122663
PheGenIrs398122663
hapmaprs398122663
1000 genomesrs398122663
hgdprs398122663
ensemblrs398122663
gopubmedrs398122663
geneviewrs398122663
scholarrs398122663
googlers398122663
pharmgkbrs398122663
gwascentralrs398122663
openSNPrs398122663
23andMers398122663
23andMe allrs398122663
SNP Nexus

SNPshotrs398122663
SNPdbers398122663
MSV3drs398122663
GWAS Ctlgrs398122663
Max Magnitude0
ClinVar
Risk rs398122663(;)
Alt rs398122663(;)
Reference rs398122663(T;T)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA1
CLNDBN Breast-ovarian cancer, familial 1
Reversed 1
HGVS NC_000017.10:g.41244894delA
CLNSRC ClinVar
CLNACC RCV000077112.2,