Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs61748420
rs61748420
MECP2
CUI: C3714756
Disease: Intellectual Disability
Intellectual Disability 		0.020 GeneticVariation BEFREE Targeted next-generation sequencing of a panel of intellectual disability related genes was performed on two unrelated male patients, and two missense variants in MECP2 were identified (p.Gly185Val and p.Arg167Trp). 26490184

2016
dbSNP: rs61748420
rs61748420
MECP2
CUI: C3714756
Disease: Intellectual Disability
Intellectual Disability 		0.020 GeneticVariation BEFREE The first mutation, an E137G, was identified in the MRX16 family, and the second, R167W, was identified in a new mental retardation (MR) family shown to be linked to Xq28. 11309367

2001