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rs398122631

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs398122631(-;-)
Make rs398122631(-;A)
Make rs398122631(A;A)
ReferenceGRCh38 38.1/141
Chromosome17
Position43094194
GeneBRCA1
is asnp
is mentioned by
dbSNPrs398122631
ebirs398122631
HLIrs398122631
Exacrs398122631
Varsomers398122631
Maprs398122631
PheGenIrs398122631
hapmaprs398122631
1000 genomesrs398122631
hgdprs398122631
ensemblrs398122631
gopubmedrs398122631
geneviewrs398122631
scholarrs398122631
googlers398122631
pharmgkbrs398122631
gwascentralrs398122631
openSNPrs398122631
23andMers398122631
23andMe allrs398122631
SNP Nexus

SNPshotrs398122631
SNPdbers398122631
MSV3drs398122631
GWAS Ctlgrs398122631
Max Magnitude0
ClinVar
Risk rs398122631(A;A)
Alt rs398122631(A;A)
Reference rs398122631(;)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA1
CLNDBN Breast-ovarian cancer, familial 1
Reversed 1
HGVS NC_000017.10:g.41246212dupT
CLNSRC ClinVar
CLNACC RCV000077063.2,