Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs878853263
rs878853263
ARHGAP4 ; NAA10
CUI: C3275447
Disease: Ogden syndrome
Ogden syndrome 		T 0.700 CausalMutation CLINVAR

dbSNP: rs878853263
rs878853263
ARHGAP4 ; NAA10
CUI: C3275447
Disease: Ogden syndrome
Ogden syndrome 		C 0.700 CausalMutation CLINVAR