Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs387906701
rs387906701
ARHGAP4 ; NAA10
CUI: C3275447
Disease: Ogden syndrome
Ogden syndrome 		G 0.840 CausalMutation CLINVAR

dbSNP: rs863225427
rs863225427
ARHGAP4 ; NAA10
CUI: C3275447
Disease: Ogden syndrome
Ogden syndrome 		G 0.810 CausalMutation CLINVAR

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

dbSNP: rs1057524031
rs1057524031
ARHGAP4 ; NAA10
CUI: C1843367
Disease: Poor school performance
Poor school performance 		A 0.700 GeneticVariation CLINVAR

dbSNP: rs1557107462
rs1557107462
ARHGAP4 ; NAA10
CUI: C3275447
Disease: Ogden syndrome
Ogden syndrome 		C 0.700 GeneticVariation CLINVAR

dbSNP: rs1557107528
rs1557107528
ARHGAP4 ; NAA10
CUI: C3275447
Disease: Ogden syndrome
Ogden syndrome 		C 0.700 CausalMutation CLINVAR

dbSNP: rs1557107528
rs1557107528
ARHGAP4 ; NAA10
CUI: C1843367
Disease: Poor school performance
Poor school performance 		C 0.700 CausalMutation CLINVAR

dbSNP: rs1557107543
rs1557107543
ARHGAP4 ; NAA10
CUI: C3275447
Disease: Ogden syndrome
Ogden syndrome 		A 0.700 GeneticVariation CLINVAR

dbSNP: rs1569546255
rs1569546255
ARHGAP4 ; NAA10
CUI: C3275447
Disease: Ogden syndrome
Ogden syndrome 		C 0.700 CausalMutation CLINVAR

dbSNP: rs587776457
rs587776457
ARHGAP4 ; NAA10
CUI: C0796016
Disease: Microphthalmia, syndromic 1
Microphthalmia, syndromic 1 		T 0.700 CausalMutation CLINVAR

dbSNP: rs587780562
rs587780562
ARHGAP4 ; NAA10
CUI: C3275447
Disease: Ogden syndrome
Ogden syndrome 		A 0.700 CausalMutation CLINVAR

dbSNP: rs587780563
rs587780563
ARHGAP4 ; NAA10
CUI: C3275447
Disease: Ogden syndrome
Ogden syndrome 		A 0.700 CausalMutation CLINVAR

dbSNP: rs797044868
rs797044868
ARHGAP4 ; NAA10
CUI: C3275447
Disease: Ogden syndrome
Ogden syndrome 		A 0.700 CausalMutation CLINVAR

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

dbSNP: rs878853264
rs878853264
ARHGAP4 ; NAA10
CUI: C1843367
Disease: Poor school performance
Poor school performance 		T 0.700 GeneticVariation CLINVAR

dbSNP: rs878853264
rs878853264
ARHGAP4 ; NAA10
CUI: C3275447
Disease: Ogden syndrome
Ogden syndrome 		T 0.700 CausalMutation CLINVAR