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rs398122657

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs398122657(-;-)
Make rs398122657(-;A)
Make rs398122657(A;A)
ReferenceGRCh38 38.1/141
Chromosome17
Position43093144
GeneBRCA1
is asnp
is mentioned by
dbSNPrs398122657
ebirs398122657
HLIrs398122657
Exacrs398122657
Varsomers398122657
Maprs398122657
PheGenIrs398122657
hapmaprs398122657
1000 genomesrs398122657
hgdprs398122657
ensemblrs398122657
gopubmedrs398122657
geneviewrs398122657
scholarrs398122657
googlers398122657
pharmgkbrs398122657
gwascentralrs398122657
openSNPrs398122657
23andMers398122657
23andMe allrs398122657
SNP Nexus

SNPshotrs398122657
SNPdbers398122657
MSV3drs398122657
GWAS Ctlgrs398122657
Max Magnitude0
ClinVar
Risk rs398122657(A;A)
Alt rs398122657(A;A)
Reference rs398122657(;)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene BRCA1
CLNDBN Breast-ovarian cancer, familial 1
Reversed 1
HGVS NC_000017.10:g.41245162dupT
CLNSRC ClinVar
CLNACC RCV000077102.2,