Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 32 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs763353895
rs763353895
Entrez Id: 3737
Gene Symbol: KCNA2
KCNA2
CUI: C4225350
Disease:
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 32 		A 0.700 CausalMutation CLINVAR Exome sequencing of Pakistani consanguineous families identifies 30 novel candidate genes for recessive intellectual disability. 27457812 2017