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rs398122636

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs398122636(-;-)
Make rs398122636(-;T)
Make rs398122636(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43094018
GeneBRCA1
is asnp
is mentioned by
dbSNPrs398122636
ebirs398122636
HLIrs398122636
Exacrs398122636
Varsomers398122636
Maprs398122636
PheGenIrs398122636
hapmaprs398122636
1000 genomesrs398122636
hgdprs398122636
ensemblrs398122636
gopubmedrs398122636
geneviewrs398122636
scholarrs398122636
googlers398122636
pharmgkbrs398122636
gwascentralrs398122636
openSNPrs398122636
23andMers398122636
23andMe allrs398122636
SNP Nexus

SNPshotrs398122636
SNPdbers398122636
MSV3drs398122636
GWAS Ctlgrs398122636
Max Magnitude0
ClinVar
Risk rs398122636(T;T)
Alt rs398122636(T;T)
Reference rs398122636(;)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA1
CLNDBN Breast-ovarian cancer, familial 1
Reversed 1
HGVS NC_000017.10:g.41246036dupA
CLNSRC ClinVar
CLNACC RCV000077071.2,