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rs876658947

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876658947(-;-)
Make rs876658947(-;A)
Make rs876658947(A;A)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position43067684
GeneBRCA1
is asnp
is mentioned by
dbSNPrs876658947
ebirs876658947
HLIrs876658947
Exacrs876658947
Varsomers876658947
Maprs876658947
PheGenIrs876658947
hapmaprs876658947
1000 genomesrs876658947
hgdprs876658947
ensemblrs876658947
gopubmedrs876658947
geneviewrs876658947
scholarrs876658947
googlers876658947
pharmgkbrs876658947
gwascentralrs876658947
openSNPrs876658947
23andMers876658947
23andMe allrs876658947
SNP Nexus

SNPshotrs876658947
SNPdbers876658947
MSV3drs876658947
GWAS Ctlgrs876658947
Max Magnitude0
ClinVar
Risk rs876658947(A;A)
Alt rs876658947(A;A)
Reference rs876658947(;)
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.41219702dupT
CLNSRC
CLNACC RCV000220908.1,