rs1553602821
×
Entrez Id:
9320
Gene Symbol:
TRIP12
TRIP12
MENTAL RETARDATION, AUTOSOMAL DOMINANT 49
0.800
GeneticVariation
UNIPROT
Identification of new TRIP12 variants and detailed clinical evaluation of individuals with non-syndromic intellectual disability with or without autism.
27848077
2017
rs1553602821
×
Entrez Id:
9320
Gene Symbol:
TRIP12
TRIP12
MENTAL RETARDATION, AUTOSOMAL DOMINANT 49
0.800
GeneticVariation
UNIPROT
Haploinsufficiency of the E3 ubiquitin-protein ligase gene TRIP12 causes intellectual disability with or without autism spectrum disorders, speech delay, and dysmorphic features.
28251352
2017
rs1553602821
×
Entrez Id:
9320
Gene Symbol:
TRIP12
TRIP12
MENTAL RETARDATION, AUTOSOMAL DOMINANT 49
T
0.800
CausalMutation
CLINVAR
rs1044822
×
Entrez Id:
9320
Gene Symbol:
TRIP12
TRIP12
Systolic Pressure
T
0.700
GeneticVariation
GWASCAT
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits.
30224653
2018
rs1300458163
×
Entrez Id:
9320
Gene Symbol:
TRIP12
TRIP12
MENTAL RETARDATION, AUTOSOMAL DOMINANT 49
0.700
GeneticVariation
UNIPROT
Identification of new TRIP12 variants and detailed clinical evaluation of individuals with non-syndromic intellectual disability with or without autism.
27848077
2017
rs1300458163
×
Entrez Id:
9320
Gene Symbol:
TRIP12
TRIP12
MENTAL RETARDATION, AUTOSOMAL DOMINANT 49
0.700
GeneticVariation
UNIPROT
Haploinsufficiency of the E3 ubiquitin-protein ligase gene TRIP12 causes intellectual disability with or without autism spectrum disorders, speech delay, and dysmorphic features.
28251352
2017
rs1553612358
×
Entrez Id:
9320
Gene Symbol:
TRIP12
TRIP12
MENTAL RETARDATION, AUTOSOMAL DOMINANT 49
T
0.700
CausalMutation
CLINVAR
rs1553614300
×
Entrez Id:
9320
Gene Symbol:
TRIP12
TRIP12
MENTAL RETARDATION, AUTOSOMAL DOMINANT 49
C
0.700
CausalMutation
CLINVAR
rs1553616463
×
Entrez Id:
9320
Gene Symbol:
TRIP12
TRIP12
MENTAL RETARDATION, AUTOSOMAL DOMINANT 49
T
0.700
CausalMutation
CLINVAR
rs1553620494
×
Entrez Id:
9320
Gene Symbol:
TRIP12
TRIP12
MENTAL RETARDATION, AUTOSOMAL DOMINANT 49
CT
0.700
CausalMutation
CLINVAR
rs1553655558
×
Entrez Id:
9320
Gene Symbol:
TRIP12
TRIP12
Severe intellectual disability
G
0.700
CausalMutation
CLINVAR
rs1553655558
×
Entrez Id:
9320
Gene Symbol:
TRIP12
TRIP12
Small for gestational age (disorder)
G
0.700
CausalMutation
CLINVAR
rs1553655558
×
Entrez Id:
9320
Gene Symbol:
TRIP12
TRIP12
Micrognathism
G
0.700
CausalMutation
CLINVAR
rs1553655558
×
Entrez Id:
9320
Gene Symbol:
TRIP12
TRIP12
Constipation
G
0.700
CausalMutation
CLINVAR
rs1553655558
×
Entrez Id:
9320
Gene Symbol:
TRIP12
TRIP12
Broad toe
G
0.700
CausalMutation
CLINVAR
rs1553655558
×
Entrez Id:
9320
Gene Symbol:
TRIP12
TRIP12
Meconium ileus
G
0.700
CausalMutation
CLINVAR
rs1553655558
×
Entrez Id:
9320
Gene Symbol:
TRIP12
TRIP12
Delayed speech and language development
G
0.700
CausalMutation
CLINVAR
rs1553655558
×
Entrez Id:
9320
Gene Symbol:
TRIP12
TRIP12
Fragile nails
G
0.700
CausalMutation
CLINVAR
rs1553655558
×
Entrez Id:
9320
Gene Symbol:
TRIP12
TRIP12
Apnea
G
0.700
CausalMutation
CLINVAR
rs1553655558
×
Entrez Id:
9320
Gene Symbol:
TRIP12
TRIP12
Head Banging
G
0.700
CausalMutation
CLINVAR
rs1553655558
×
Entrez Id:
9320
Gene Symbol:
TRIP12
TRIP12
Short stature
G
0.700
CausalMutation
CLINVAR
rs1553655558
×
Entrez Id:
9320
Gene Symbol:
TRIP12
TRIP12
Trigonocephaly
G
0.700
CausalMutation
CLINVAR
rs1553655558
×
Entrez Id:
9320
Gene Symbol:
TRIP12
TRIP12
Weight less than 3rd percentile
G
0.700
CausalMutation
CLINVAR
rs1553655558
×
Entrez Id:
9320
Gene Symbol:
TRIP12
TRIP12
Narrow forehead
G
0.700
CausalMutation
CLINVAR
rs1553655558
×
Entrez Id:
9320
Gene Symbol:
TRIP12
TRIP12
Downturned corners of mouth
G
0.700
CausalMutation
CLINVAR