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rs374435098

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs374435098(C;T)
Make rs374435098(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position43079400
GeneBRCA1
is asnp
is mentioned by
dbSNPrs374435098
ebirs374435098
HLIrs374435098
Exacrs374435098
Varsomers374435098
Maprs374435098
PheGenIrs374435098
hapmaprs374435098
1000 genomesrs374435098
hgdprs374435098
ensemblrs374435098
gopubmedrs374435098
geneviewrs374435098
scholarrs374435098
googlers374435098
pharmgkbrs374435098
gwascentralrs374435098
openSNPrs374435098
23andMers374435098
23andMe allrs374435098
SNP Nexus

SNPshotrs374435098
SNPdbers374435098
MSV3drs374435098
GWAS Ctlgrs374435098
Max Magnitude0
ClinVar
Risk rs374435098(T;T)
Alt rs374435098(T;T)
Reference rs374435098(C;C)
Significance Probable-Pathogenic
Disease Hereditary breast and ovarian cancer syndrome
Variation info
Gene BRCA1
CLNDBN Hereditary breast and ovarian cancer syndrome
Reversed 0
HGVS NC_000017.10:g.41231417C>T
CLNSRC
CLNACC RCV000149888.1,