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rs876658361

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876658361(-;-)
Make rs876658361(-;C)
Make rs876658361(C;C)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position43093097
GeneBRCA1
is asnp
is mentioned by
dbSNPrs876658361
ebirs876658361
HLIrs876658361
Exacrs876658361
Varsomers876658361
Maprs876658361
PheGenIrs876658361
hapmaprs876658361
1000 genomesrs876658361
hgdprs876658361
ensemblrs876658361
gopubmedrs876658361
geneviewrs876658361
scholarrs876658361
googlers876658361
pharmgkbrs876658361
gwascentralrs876658361
openSNPrs876658361
23andMers876658361
23andMe allrs876658361
SNP Nexus

SNPshotrs876658361
SNPdbers876658361
MSV3drs876658361
GWAS Ctlgrs876658361
Max Magnitude0
ClinVar
Risk rs876658361(C;C)
Alt rs876658361(C;C)
Reference rs876658361(;)
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.41245115dupG
CLNSRC
CLNACC RCV000214256.1,