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rs876659457

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs876659457(A;T)
Make rs876659457(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position43092851
GeneBRCA1
is asnp
is mentioned by
dbSNPrs876659457
ebirs876659457
HLIrs876659457
Exacrs876659457
Varsomers876659457
Maprs876659457
PheGenIrs876659457
hapmaprs876659457
1000 genomesrs876659457
hgdprs876659457
ensemblrs876659457
gopubmedrs876659457
geneviewrs876659457
scholarrs876659457
googlers876659457
pharmgkbrs876659457
gwascentralrs876659457
openSNPrs876659457
23andMers876659457
23andMe allrs876659457
SNP Nexus

SNPshotrs876659457
SNPdbers876659457
MSV3drs876659457
GWAS Ctlgrs876659457
Max Magnitude0
ClinVar
Risk rs876659457(T;T)
Alt rs876659457(T;T)
Reference rs876659457(A;A)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene BRCA1
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 1
HGVS NC_000017.10:g.41244868T>A
CLNSRC
CLNACC RCV000221767.1,