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rs876659072

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs876659072(-;-)
Make rs876659072(-;A)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position43092814
GeneBRCA1
is asnp
is mentioned by
dbSNPrs876659072
ebirs876659072
HLIrs876659072
Exacrs876659072
Varsomers876659072
Maprs876659072
PheGenIrs876659072
hapmaprs876659072
1000 genomesrs876659072
hgdprs876659072
ensemblrs876659072
gopubmedrs876659072
geneviewrs876659072
scholarrs876659072
googlers876659072
pharmgkbrs876659072
gwascentralrs876659072
openSNPrs876659072
23andMers876659072
23andMe allrs876659072
SNP Nexus

SNPshotrs876659072
SNPdbers876659072
MSV3drs876659072
GWAS Ctlgrs876659072
Max Magnitude0
ClinVar
Risk rs876659072(;)
Alt rs876659072(;)
Reference rs876659072(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.41244831delT
CLNSRC
CLNACC RCV000219226.1,