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rs876659136

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876659136(-;-)
Make rs876659136(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position43093169
GeneBRCA1
is asnp
is mentioned by
dbSNPrs876659136
ebirs876659136
HLIrs876659136
Exacrs876659136
Varsomers876659136
Maprs876659136
PheGenIrs876659136
hapmaprs876659136
1000 genomesrs876659136
hgdprs876659136
ensemblrs876659136
gopubmedrs876659136
geneviewrs876659136
scholarrs876659136
googlers876659136
pharmgkbrs876659136
gwascentralrs876659136
openSNPrs876659136
23andMers876659136
23andMe allrs876659136
SNP Nexus

SNPshotrs876659136
SNPdbers876659136
MSV3drs876659136
GWAS Ctlgrs876659136
Max Magnitude0
ClinVar
Risk rs876659136(;)
Alt rs876659136(;)
Reference rs876659136(G;G)
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.41245186delC
CLNSRC
CLNACC RCV000213583.1,