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rs876658791

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876658791(-;-)
Make rs876658791(-;T)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position43093242
GeneBRCA1
is asnp
is mentioned by
dbSNPrs876658791
ebirs876658791
HLIrs876658791
Exacrs876658791
Varsomers876658791
Maprs876658791
PheGenIrs876658791
hapmaprs876658791
1000 genomesrs876658791
hgdprs876658791
ensemblrs876658791
gopubmedrs876658791
geneviewrs876658791
scholarrs876658791
googlers876658791
pharmgkbrs876658791
gwascentralrs876658791
openSNPrs876658791
23andMers876658791
23andMe allrs876658791
SNP Nexus

SNPshotrs876658791
SNPdbers876658791
MSV3drs876658791
GWAS Ctlgrs876658791
Max Magnitude0
ClinVar
Risk rs876658791(;)
Alt rs876658791(;)
Reference rs876658791(T;T)
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.41245259delA
CLNSRC
CLNACC RCV000220988.1,