PRDM8, PR/SET domain 8, 56978

N. diseases: 39; N. variants: 1
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs863225286
rs863225286
Entrez Id: 56978
Gene Symbol: PRDM8
PRDM8
CUI: C4225258
Disease:
EPILEPSY, PROGRESSIVE MYOCLONIC, 10 		0.800 GeneticVariation UNIPROT
dbSNP: rs863225286
rs863225286
Entrez Id: 56978
Gene Symbol: PRDM8
PRDM8
CUI: C4225258
Disease:
EPILEPSY, PROGRESSIVE MYOCLONIC, 10 		C 0.800 CausalMutation CLINVAR