Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057519448
rs1057519448
ARHGAP4 ; NAA10
CUI: C3275447
Disease: Ogden syndrome
Ogden syndrome 		G 0.700 GeneticVariation CLINVAR Lessons learned from additional research analyses of unsolved clinical exome cases. 28327206

2017
dbSNP: rs1057519448
rs1057519448
ARHGAP4 ; NAA10
CUI: C3275447
Disease: Ogden syndrome
Ogden syndrome 		G 0.700 CausalMutation CLINVAR