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rs876659830

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876659830(-;-)
Make rs876659830(-;C)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position43099866
GeneBRCA1
is asnp
is mentioned by
dbSNPrs876659830
ebirs876659830
HLIrs876659830
Exacrs876659830
Varsomers876659830
Maprs876659830
PheGenIrs876659830
hapmaprs876659830
1000 genomesrs876659830
hgdprs876659830
ensemblrs876659830
gopubmedrs876659830
geneviewrs876659830
scholarrs876659830
googlers876659830
pharmgkbrs876659830
gwascentralrs876659830
openSNPrs876659830
23andMers876659830
23andMe allrs876659830
SNP Nexus

SNPshotrs876659830
SNPdbers876659830
MSV3drs876659830
GWAS Ctlgrs876659830
Max Magnitude0
ClinVar
Risk rs876659830(;)
Alt rs876659830(;)
Reference rs876659830(C;C)
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.41251883delG
CLNSRC
CLNACC RCV000221805.1,