MYH9, myosin heavy chain 9, 4627

N. diseases: 196; N. variants: 38
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs80338831
rs80338831
Entrez Id: 4627
Gene Symbol: MYH9
MYH9
CUI: C0340978
Disease:
May-Hegglin anomaly
A 0.830 CausalMutation CLINVAR
dbSNP: rs80338831
rs80338831
Entrez Id: 4627
Gene Symbol: MYH9
MYH9
CUI: C0340978
Disease:
May-Hegglin anomaly
G 0.830 CausalMutation CLINVAR
dbSNP: rs80338831
rs80338831
Entrez Id: 4627
Gene Symbol: MYH9
MYH9
CUI: C0340978
Disease:
May-Hegglin anomaly
T 0.830 CausalMutation CLINVAR
dbSNP: rs80338834
rs80338834
Entrez Id: 4627
Gene Symbol: MYH9
MYH9
CUI: C0340978
Disease:
May-Hegglin anomaly
T 0.830 CausalMutation CLINVAR
dbSNP: rs80338826
rs80338826
Entrez Id: 4627
Gene Symbol: MYH9
MYH9
CUI: C0340978
Disease:
May-Hegglin anomaly
A 0.810 CausalMutation CLINVAR
dbSNP: rs80338827
rs80338827
Entrez Id: 4627
Gene Symbol: MYH9
MYH9
CUI: C0340978
Disease:
May-Hegglin anomaly
T 0.810 CausalMutation CLINVAR
dbSNP: rs80338828
rs80338828
Entrez Id: 4627
Gene Symbol: MYH9
MYH9
CUI: C1863659
Disease:
DEAFNESS, AUTOSOMAL DOMINANT 17
T 0.810 CausalMutation CLINVAR
dbSNP: rs121913655
rs121913655
Entrez Id: 4627
Gene Symbol: MYH9
MYH9
CUI: C0340978
Disease:
May-Hegglin anomaly
C 0.800 CausalMutation CLINVAR
dbSNP: rs121913656
rs121913656
Entrez Id: 4627
Gene Symbol: MYH9
MYH9
CUI: C0340978
Disease:
May-Hegglin anomaly
A 0.800 CausalMutation CLINVAR
dbSNP: rs121913657
rs121913657
Entrez Id: 4627
Gene Symbol: MYH9
MYH9
CUI: C0340978
Disease:
May-Hegglin anomaly
A 0.800 CausalMutation CLINVAR
dbSNP: rs80338829
rs80338829
Entrez Id: 4627
Gene Symbol: MYH9
MYH9
CUI: C0340978
Disease:
May-Hegglin anomaly
A 0.800 CausalMutation CLINVAR
dbSNP: rs80338830
rs80338830
Entrez Id: 4627
Gene Symbol: MYH9
MYH9
CUI: C0340978
Disease:
May-Hegglin anomaly
A 0.800 CausalMutation CLINVAR
dbSNP: rs80338835
rs80338835
Entrez Id: 4627
Gene Symbol: MYH9
MYH9
CUI: C0340978
Disease:
May-Hegglin anomaly
A 0.730 CausalMutation CLINVAR
dbSNP: rs80338831
rs80338831
Entrez Id: 4627
Gene Symbol: MYH9
MYH9
CUI: C1854520
Disease:
SEBASTIAN SYNDROME
T 0.720 CausalMutation CLINVAR
dbSNP: rs80338831
rs80338831
Entrez Id: 4627
Gene Symbol: MYH9
MYH9
CUI: C1854520
Disease:
SEBASTIAN SYNDROME
A 0.720 CausalMutation CLINVAR
dbSNP: rs121913657
rs121913657
Entrez Id: 4627
Gene Symbol: MYH9
MYH9
CUI: C1854520
Disease:
SEBASTIAN SYNDROME
A 0.710 CausalMutation CLINVAR
dbSNP: rs80338826
rs80338826
Entrez Id: 4627
Gene Symbol: MYH9
MYH9
CUI: C1854520
Disease:
SEBASTIAN SYNDROME
A 0.710 CausalMutation CLINVAR
dbSNP: rs80338829
rs80338829
Entrez Id: 4627
Gene Symbol: MYH9
MYH9
CUI: C1854520
Disease:
SEBASTIAN SYNDROME
A 0.710 CausalMutation CLINVAR
dbSNP: rs80338834
rs80338834
Entrez Id: 4627
Gene Symbol: MYH9
MYH9
CUI: C1854520
Disease:
SEBASTIAN SYNDROME
T 0.710 CausalMutation CLINVAR
dbSNP: rs80338835
rs80338835
Entrez Id: 4627
Gene Symbol: MYH9
MYH9
CUI: C1854520
Disease:
SEBASTIAN SYNDROME
A 0.710 CausalMutation CLINVAR
dbSNP: rs121913655
rs121913655
Entrez Id: 4627
Gene Symbol: MYH9
MYH9
CUI: C1854520
Disease:
SEBASTIAN SYNDROME
C 0.700 CausalMutation CLINVAR
dbSNP: rs1430793034
rs1430793034
Entrez Id: 4627
Gene Symbol: MYH9
MYH9
CUI: C1865871
Disease:
HEMANGIOMA, CAPILLARY INFANTILE
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1430793034
rs1430793034
Entrez Id: 4627
Gene Symbol: MYH9
MYH9
CUI: C1842774
Disease:
Hypermelanotic macule
A 0.700 GeneticVariation CLINVAR
dbSNP: rs587776808
rs587776808
Entrez Id: 4627
Gene Symbol: MYH9
MYH9
CUI: C0340978
Disease:
May-Hegglin anomaly
T 0.700 CausalMutation CLINVAR
dbSNP: rs797044804
rs797044804
Entrez Id: 4627
Gene Symbol: MYH9
MYH9
CUI: C1854520
Disease:
SEBASTIAN SYNDROME
A 0.700 GeneticVariation CLINVAR