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rs398122664

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs398122664(-;-)
Make rs398122664(-;A)
Make rs398122664(A;A)
ReferenceGRCh38 38.1/141
Chromosome17
Position43092844
GeneBRCA1
is asnp
is mentioned by
dbSNPrs398122664
ebirs398122664
HLIrs398122664
Exacrs398122664
Varsomers398122664
Maprs398122664
PheGenIrs398122664
hapmaprs398122664
1000 genomesrs398122664
hgdprs398122664
ensemblrs398122664
gopubmedrs398122664
geneviewrs398122664
scholarrs398122664
googlers398122664
pharmgkbrs398122664
gwascentralrs398122664
openSNPrs398122664
23andMers398122664
23andMe allrs398122664
SNP Nexus

SNPshotrs398122664
SNPdbers398122664
MSV3drs398122664
GWAS Ctlgrs398122664
Max Magnitude0
ClinVar
Risk rs398122664(A;A)
Alt rs398122664(A;A)
Reference rs398122664(;)
Significance Pathogenic
Disease Breast-ovarian cancer Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA1
CLNDBN Breast-ovarian cancer, familial 1 Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.41244862dupT
CLNSRC ClinVar
CLNACC RCV000077113.2, RCV000165785.1,