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rs876660523

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876660523(-;-)
Make rs876660523(-;G)
Make rs876660523(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position43093694
GeneBRCA1
is asnp
is mentioned by
dbSNPrs876660523
ebirs876660523
HLIrs876660523
Exacrs876660523
Varsomers876660523
Maprs876660523
PheGenIrs876660523
hapmaprs876660523
1000 genomesrs876660523
hgdprs876660523
ensemblrs876660523
gopubmedrs876660523
geneviewrs876660523
scholarrs876660523
googlers876660523
pharmgkbrs876660523
gwascentralrs876660523
openSNPrs876660523
23andMers876660523
23andMe allrs876660523
SNP Nexus

SNPshotrs876660523
SNPdbers876660523
MSV3drs876660523
GWAS Ctlgrs876660523
Max Magnitude0
ClinVar
Risk rs876660523(G;G)
Alt rs876660523(G;G)
Reference rs876660523(;)
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.41245712dupC
CLNSRC
CLNACC RCV000217364.1,