Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs267606828
rs267606828
FOXG1
CUI: C3150705
Disease: FOXG1 syndrome
FOXG1 syndrome 		C 0.800 CausalMutation CLINVAR

dbSNP: rs879255530
rs879255530
FOXG1
CUI: C3150705
Disease: FOXG1 syndrome
FOXG1 syndrome 		T 0.700 GeneticVariation CLINVAR

dbSNP: rs879255530
rs879255530
FOXG1
CUI: C0856975
Disease: Autistic behavior
Autistic behavior 		T 0.700 GeneticVariation CLINVAR

dbSNP: rs869312700
rs869312700
FOXG1
CUI: C0026351
Disease: Moderate intellectual disability
Moderate intellectual disability 		A 0.700 CausalMutation CLINVAR

dbSNP: rs869312700
rs869312700
FOXG1
CUI: C3150705
Disease: FOXG1 syndrome
FOXG1 syndrome 		A 0.700 CausalMutation CLINVAR

dbSNP: rs869312700
rs869312700
FOXG1
CUI: C0454644
Disease: Delayed speech and language development
Delayed speech and language development 		A 0.700 CausalMutation CLINVAR

dbSNP: rs796052469
rs796052469
FOXG1
CUI: C3150705
Disease: FOXG1 syndrome
FOXG1 syndrome 		A 0.700 GeneticVariation CLINVAR

dbSNP: rs786205486
rs786205486
FOXG1
CUI: C3150705
Disease: FOXG1 syndrome
FOXG1 syndrome 		G 0.700 GeneticVariation CLINVAR

dbSNP: rs786205011
rs786205011
FOXG1
CUI: C3150705
Disease: FOXG1 syndrome
FOXG1 syndrome 		G 0.700 CausalMutation CLINVAR

dbSNP: rs786205010
rs786205010
FOXG1
CUI: C3150705
Disease: FOXG1 syndrome
FOXG1 syndrome 		C 0.700 CausalMutation CLINVAR

dbSNP: rs786205008
rs786205008
FOXG1
CUI: C3150705
Disease: FOXG1 syndrome
FOXG1 syndrome 		C 0.700 CausalMutation CLINVAR

dbSNP: rs786205007
rs786205007
FOXG1
CUI: C3150705
Disease: FOXG1 syndrome
FOXG1 syndrome 		A 0.700 CausalMutation CLINVAR

dbSNP: rs786205005
rs786205005
FOXG1
CUI: C3150705
Disease: FOXG1 syndrome
FOXG1 syndrome 		A 0.700 CausalMutation CLINVAR

dbSNP: rs786205004
rs786205004
FOXG1
CUI: C3150705
Disease: FOXG1 syndrome
FOXG1 syndrome 		TC 0.700 CausalMutation CLINVAR

dbSNP: rs786205003
rs786205003
FOXG1
CUI: C3150705
Disease: FOXG1 syndrome
FOXG1 syndrome 		T 0.700 CausalMutation CLINVAR

dbSNP: rs786205003
rs786205003
FOXG1
CUI: C3150705
Disease: FOXG1 syndrome
FOXG1 syndrome 		C 0.700 CausalMutation CLINVAR

dbSNP: rs786205001
rs786205001
FOXG1
CUI: C3150705
Disease: FOXG1 syndrome
FOXG1 syndrome 		GC 0.700 CausalMutation CLINVAR

dbSNP: rs786204999
rs786204999
FOXG1
CUI: C3150705
Disease: FOXG1 syndrome
FOXG1 syndrome 		G 0.700 CausalMutation CLINVAR

dbSNP: rs786204998
rs786204998
FOXG1
CUI: C3150705
Disease: FOXG1 syndrome
FOXG1 syndrome 		CT 0.700 GeneticVariation CLINVAR

dbSNP: rs727503935
rs727503935
FOXG1
CUI: C3150705
Disease: FOXG1 syndrome
FOXG1 syndrome 		A 0.700 GeneticVariation CLINVAR

dbSNP: rs587783643
rs587783643
FOXG1
CUI: C3150705
Disease: FOXG1 syndrome
FOXG1 syndrome 		A 0.700 GeneticVariation CLINVAR

dbSNP: rs587783642
rs587783642
FOXG1
CUI: C3150705
Disease: FOXG1 syndrome
FOXG1 syndrome 		G 0.700 CausalMutation CLINVAR

dbSNP: rs587783641
rs587783641
FOXG1
CUI: C3150705
Disease: FOXG1 syndrome
FOXG1 syndrome 		G 0.700 CausalMutation CLINVAR

dbSNP: rs587783640
rs587783640
FOXG1
CUI: C3150705
Disease: FOXG1 syndrome
FOXG1 syndrome 		T 0.700 GeneticVariation CLINVAR

dbSNP: rs587783636
rs587783636
FOXG1
CUI: C3150705
Disease: FOXG1 syndrome
FOXG1 syndrome 		G 0.700 CausalMutation CLINVAR