Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1556909287
rs1556909287
Entrez Id: 10075
Gene Symbol: HUWE1
HUWE1
CUI: C2678046
Disease:
Mental Retardation, X-Linked, Syndromic, Turner Type
G 0.700 CausalMutation CLINVAR HUWE1 mutations in Juberg-Marsidi and Brooks syndromes: the results of an X-chromosome exome sequencing study. 27130160 2016
dbSNP: rs1057518704
rs1057518704
Entrez Id: 10075
Gene Symbol: HUWE1
HUWE1
CUI: C2678046
Disease:
Mental Retardation, X-Linked, Syndromic, Turner Type
T 0.700 GeneticVariation CLINVAR
dbSNP: rs1057520538
rs1057520538
Entrez Id: 10075
Gene Symbol: HUWE1
HUWE1
CUI: C2678046
Disease:
Mental Retardation, X-Linked, Syndromic, Turner Type
A 0.700 CausalMutation CLINVAR
dbSNP: rs121918525
rs121918525
Entrez Id: 10075
Gene Symbol: HUWE1
HUWE1
CUI: C2678046
Disease:
Mental Retardation, X-Linked, Syndromic, Turner Type
A 0.700 CausalMutation CLINVAR
dbSNP: rs121918526
rs121918526
Entrez Id: 10075
Gene Symbol: HUWE1
HUWE1
CUI: C2678046
Disease:
Mental Retardation, X-Linked, Syndromic, Turner Type
T 0.700 CausalMutation CLINVAR
dbSNP: rs121918527
rs121918527
Entrez Id: 10075
Gene Symbol: HUWE1
HUWE1
CUI: C2678046
Disease:
Mental Retardation, X-Linked, Syndromic, Turner Type
A 0.700 CausalMutation CLINVAR
dbSNP: rs1325394060
rs1325394060
Entrez Id: 10075
Gene Symbol: HUWE1
HUWE1
CUI: C1854882
Disease:
Absent speech
G 0.700 GeneticVariation CLINVAR
dbSNP: rs1325394060
rs1325394060
Entrez Id: 10075
Gene Symbol: HUWE1
HUWE1
CUI: C0036857
Disease:
Severe intellectual disability
G 0.700 GeneticVariation CLINVAR
dbSNP: rs1325394060
rs1325394060
Entrez Id: 10075
Gene Symbol: HUWE1
HUWE1
CUI: C2678046
Disease:
Mental Retardation, X-Linked, Syndromic, Turner Type
G 0.700 GeneticVariation CLINVAR
dbSNP: rs1325394060
rs1325394060
Entrez Id: 10075
Gene Symbol: HUWE1
HUWE1
CUI: C0575802
Disease:
Small hand
G 0.700 GeneticVariation CLINVAR
dbSNP: rs1325394060
rs1325394060
Entrez Id: 10075
Gene Symbol: HUWE1
HUWE1
CUI: C0423224
Disease:
Sunken eyes
G 0.700 GeneticVariation CLINVAR
dbSNP: rs1325394060
rs1325394060
Entrez Id: 10075
Gene Symbol: HUWE1
HUWE1
CUI: C0038379
Disease:
Strabismus
G 0.700 GeneticVariation CLINVAR
dbSNP: rs1325394060
rs1325394060
Entrez Id: 10075
Gene Symbol: HUWE1
HUWE1
CUI: C0036572
Disease:
Seizures
G 0.700 GeneticVariation CLINVAR
dbSNP: rs1325394060
rs1325394060
Entrez Id: 10075
Gene Symbol: HUWE1
HUWE1
CUI: C0020555
Disease:
Hypertrichosis
G 0.700 GeneticVariation CLINVAR
dbSNP: rs1325394060
rs1325394060
Entrez Id: 10075
Gene Symbol: HUWE1
HUWE1
CUI: C1835465
Disease:
Short stature, postnatal
G 0.700 GeneticVariation CLINVAR
dbSNP: rs1556910184
rs1556910184
Entrez Id: 10075
Gene Symbol: HUWE1
HUWE1
CUI: C0036857
Disease:
Severe intellectual disability
G 0.700 GeneticVariation CLINVAR
dbSNP: rs1556910184
rs1556910184
Entrez Id: 10075
Gene Symbol: HUWE1
HUWE1
CUI: C0423224
Disease:
Sunken eyes
G 0.700 GeneticVariation CLINVAR
dbSNP: rs1556910184
rs1556910184
Entrez Id: 10075
Gene Symbol: HUWE1
HUWE1
CUI: C0431352
Disease:
Secondary microcephaly
G 0.700 GeneticVariation CLINVAR
dbSNP: rs1556910184
rs1556910184
Entrez Id: 10075
Gene Symbol: HUWE1
HUWE1
CUI: C2678046
Disease:
Mental Retardation, X-Linked, Syndromic, Turner Type
G 0.700 GeneticVariation CLINVAR
dbSNP: rs1556912828
rs1556912828
Entrez Id: 10075
Gene Symbol: HUWE1
HUWE1
CUI: C0349588
Disease:
Short stature
C 0.700 GeneticVariation CLINVAR
dbSNP: rs1556912828
rs1556912828
Entrez Id: 10075
Gene Symbol: HUWE1
HUWE1
CUI: C1854882
Disease:
Absent speech
C 0.700 GeneticVariation CLINVAR
dbSNP: rs1556912828
rs1556912828
Entrez Id: 10075
Gene Symbol: HUWE1
HUWE1
CUI: C0038379
Disease:
Strabismus
C 0.700 GeneticVariation CLINVAR
dbSNP: rs1556912828
rs1556912828
Entrez Id: 10075
Gene Symbol: HUWE1
HUWE1
CUI: C2678046
Disease:
Mental Retardation, X-Linked, Syndromic, Turner Type
C 0.700 GeneticVariation CLINVAR
dbSNP: rs1556912828
rs1556912828
Entrez Id: 10075
Gene Symbol: HUWE1
HUWE1
CUI: C4551563
Disease:
Microcephaly (physical finding)
C 0.700 GeneticVariation CLINVAR
dbSNP: rs1556912828
rs1556912828
Entrez Id: 10075
Gene Symbol: HUWE1
HUWE1
CUI: C0038273
Disease:
Stereotypic Movement Disorder
C 0.700 GeneticVariation CLINVAR