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rs876659108

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876659108(-;-)
Make rs876659108(-;C)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position43092584
GeneBRCA1
is asnp
is mentioned by
dbSNPrs876659108
ebirs876659108
HLIrs876659108
Exacrs876659108
Varsomers876659108
Maprs876659108
PheGenIrs876659108
hapmaprs876659108
1000 genomesrs876659108
hgdprs876659108
ensemblrs876659108
gopubmedrs876659108
geneviewrs876659108
scholarrs876659108
googlers876659108
pharmgkbrs876659108
gwascentralrs876659108
openSNPrs876659108
23andMers876659108
23andMe allrs876659108
SNP Nexus

SNPshotrs876659108
SNPdbers876659108
MSV3drs876659108
GWAS Ctlgrs876659108
Max Magnitude0
ClinVar
Risk rs876659108(;)
Alt rs876659108(;)
Reference rs876659108(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.41244601delG
CLNSRC
CLNACC RCV000215993.1,