THOC2, THO complex 2, 57187

N. diseases: 59; N. variants: 9
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs797045018
rs797045018
Entrez Id: 57187
Gene Symbol: THOC2
THOC2
CUI: C0796218
Disease:
MENTAL RETARDATION, X-LINKED 12
G 0.800 CausalMutation CLINVAR
dbSNP: rs797045018
rs797045018
Entrez Id: 57187
Gene Symbol: THOC2
THOC2
CUI: C0796218
Disease:
MENTAL RETARDATION, X-LINKED 12
0.800 GeneticVariation UNIPROT
dbSNP: rs797045019
rs797045019
Entrez Id: 57187
Gene Symbol: THOC2
THOC2
CUI: C0796218
Disease:
MENTAL RETARDATION, X-LINKED 12
A 0.800 CausalMutation CLINVAR
dbSNP: rs797045019
rs797045019
Entrez Id: 57187
Gene Symbol: THOC2
THOC2
CUI: C0796218
Disease:
MENTAL RETARDATION, X-LINKED 12
0.800 GeneticVariation UNIPROT
dbSNP: rs797045020
rs797045020
Entrez Id: 57187
Gene Symbol: THOC2
THOC2
CUI: C0796218
Disease:
MENTAL RETARDATION, X-LINKED 12
G 0.800 CausalMutation CLINVAR
dbSNP: rs797045020
rs797045020
Entrez Id: 57187
Gene Symbol: THOC2
THOC2
CUI: C0796218
Disease:
MENTAL RETARDATION, X-LINKED 12
0.800 GeneticVariation UNIPROT
dbSNP: rs797045021
rs797045021
Entrez Id: 57187
Gene Symbol: THOC2
THOC2
CUI: C0796218
Disease:
MENTAL RETARDATION, X-LINKED 12
0.800 GeneticVariation UNIPROT
dbSNP: rs797045021
rs797045021
Entrez Id: 57187
Gene Symbol: THOC2
THOC2
CUI: C0796218
Disease:
MENTAL RETARDATION, X-LINKED 12
G 0.800 CausalMutation CLINVAR
dbSNP: rs1556005930
rs1556005930
Entrez Id: 57187
Gene Symbol: THOC2
THOC2
CUI: C0796218
Disease:
MENTAL RETARDATION, X-LINKED 12
C 0.700 GeneticVariation CLINVAR
dbSNP: rs1556014935
rs1556014935
Entrez Id: 57187
Gene Symbol: THOC2
THOC2
CUI: C0796218
Disease:
MENTAL RETARDATION, X-LINKED 12
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1556015437
rs1556015437
Entrez Id: 57187
Gene Symbol: THOC2
THOC2
CUI: C0796218
Disease:
MENTAL RETARDATION, X-LINKED 12
G 0.700 GeneticVariation CLINVAR
dbSNP: rs1556023928
rs1556023928
Entrez Id: 57187
Gene Symbol: THOC2
THOC2
CUI: C0796218
Disease:
MENTAL RETARDATION, X-LINKED 12
T 0.700 CausalMutation CLINVAR
dbSNP: rs1556024875
rs1556024875
Entrez Id: 57187
Gene Symbol: THOC2
THOC2
CUI: C0036857
Disease:
Severe intellectual disability
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1556024875
rs1556024875
Entrez Id: 57187
Gene Symbol: THOC2
THOC2
CUI: C0349588
Disease:
Short stature
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1556024875
rs1556024875
Entrez Id: 57187
Gene Symbol: THOC2
THOC2
CUI: C0796218
Disease:
MENTAL RETARDATION, X-LINKED 12
A 0.700 CausalMutation CLINVAR
dbSNP: rs1556024875
rs1556024875
Entrez Id: 57187
Gene Symbol: THOC2
THOC2
CUI: C0796218
Disease:
MENTAL RETARDATION, X-LINKED 12
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1556024875
rs1556024875
Entrez Id: 57187
Gene Symbol: THOC2
THOC2
CUI: C0432072
Disease:
Dysmorphic features
A 0.700 GeneticVariation CLINVAR