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rs876659327

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876659327(-;-)
Make rs876659327(-;G)
Make rs876659327(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position43094390
GeneBRCA1
is asnp
is mentioned by
dbSNPrs876659327
ebirs876659327
HLIrs876659327
Exacrs876659327
Varsomers876659327
Maprs876659327
PheGenIrs876659327
hapmaprs876659327
1000 genomesrs876659327
hgdprs876659327
ensemblrs876659327
gopubmedrs876659327
geneviewrs876659327
scholarrs876659327
googlers876659327
pharmgkbrs876659327
gwascentralrs876659327
openSNPrs876659327
23andMers876659327
23andMe allrs876659327
SNP Nexus

SNPshotrs876659327
SNPdbers876659327
MSV3drs876659327
GWAS Ctlgrs876659327
Max Magnitude0
ClinVar
Risk rs876659327(G;G)
Alt rs876659327(G;G)
Reference rs876659327(;)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations not provided
Variation info
Gene BRCA1
CLNDBN Tumor susceptibility linked to germline BAP1 mutations not provided
Reversed 1
HGVS NC_000017.10:g.41246408dupC
CLNSRC
CLNACC RCV000216621.1, RCV000235683.1,