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rs876659610

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876659610(A;A)
Make rs876659610(A;T)
ReferenceGRCh38.p2 38.2/147
Chromosome14
Position65077996
GeneMAX
is asnp
is mentioned by
dbSNPrs876659610
ebirs876659610
HLIrs876659610
Exacrs876659610
Varsomers876659610
Maprs876659610
PheGenIrs876659610
hapmaprs876659610
1000 genomesrs876659610
hgdprs876659610
ensemblrs876659610
gopubmedrs876659610
geneviewrs876659610
scholarrs876659610
googlers876659610
pharmgkbrs876659610
gwascentralrs876659610
openSNPrs876659610
23andMers876659610
23andMe allrs876659610
SNP Nexus

SNPshotrs876659610
SNPdbers876659610
MSV3drs876659610
GWAS Ctlgrs876659610
Max Magnitude0
ClinVar
Risk rs876659610(A;A)
Alt rs876659610(A;A)
Reference rs876659610(T;T)
Significance Probable-Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene MAX
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 1
HGVS NC_000014.8:g.65544714A>T
CLNSRC
CLNACC RCV000222188.1,