PRKCG, protein kinase C gamma, 5582

N. diseases: 90; N. variants: 35
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121918513
rs121918513
Entrez Id: 5582
Gene Symbol: PRKCG
PRKCG
CUI: C1854369
Disease:
Spinocerebellar ataxia 14
A 0.810 CausalMutation CLINVAR
dbSNP: rs121918512
rs121918512
Entrez Id: 5582
Gene Symbol: PRKCG
PRKCG
CUI: C1854369
Disease:
Spinocerebellar ataxia 14
C 0.800 CausalMutation CLINVAR
dbSNP: rs386134159
rs386134159
Entrez Id: 5582
Gene Symbol: PRKCG
PRKCG
CUI: C1854369
Disease:
Spinocerebellar ataxia 14
T 0.800 CausalMutation CLINVAR
dbSNP: rs121918518
rs121918518
Entrez Id: 5582
Gene Symbol: PRKCG
PRKCG
CUI: C1854369
Disease:
Spinocerebellar ataxia 14
G 0.720 CausalMutation CLINVAR
dbSNP: rs121918514
rs121918514
Entrez Id: 5582
Gene Symbol: PRKCG
PRKCG
CUI: C1854369
Disease:
Spinocerebellar ataxia 14
A 0.710 CausalMutation CLINVAR
dbSNP: rs121918515
rs121918515
Entrez Id: 5582
Gene Symbol: PRKCG
PRKCG
CUI: C1854369
Disease:
Spinocerebellar ataxia 14
G 0.710 CausalMutation CLINVAR
dbSNP: rs121918516
rs121918516
Entrez Id: 5582
Gene Symbol: PRKCG
PRKCG
CUI: C1854369
Disease:
Spinocerebellar ataxia 14
C 0.710 CausalMutation CLINVAR
dbSNP: rs386134168
rs386134168
Entrez Id: 5582
Gene Symbol: PRKCG
PRKCG
CUI: C1854369
Disease:
Spinocerebellar ataxia 14
A 0.710 CausalMutation CLINVAR
dbSNP: rs121918517
rs121918517
Entrez Id: 5582
Gene Symbol: PRKCG
PRKCG
CUI: C1854369
Disease:
Spinocerebellar ataxia 14
G 0.700 CausalMutation CLINVAR
dbSNP: rs1303074743
rs1303074743
Entrez Id: 5582
Gene Symbol: PRKCG
PRKCG
CUI: C1854369
Disease:
Spinocerebellar ataxia 14
T 0.700 GeneticVariation CLINVAR
dbSNP: rs1555806333
rs1555806333
Entrez Id: 5582
Gene Symbol: PRKCG
PRKCG
CUI: C1854369
Disease:
Spinocerebellar ataxia 14
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1555808841
rs1555808841
Entrez Id: 5582
Gene Symbol: PRKCG
PRKCG
CUI: C1854369
Disease:
Spinocerebellar ataxia 14
T 0.700 CausalMutation CLINVAR
dbSNP: rs386134157
rs386134157
Entrez Id: 5582
Gene Symbol: PRKCG
PRKCG
CUI: C1854369
Disease:
Spinocerebellar ataxia 14
G 0.700 CausalMutation CLINVAR
dbSNP: rs386134158
rs386134158
Entrez Id: 5582
Gene Symbol: PRKCG
PRKCG
CUI: C1854369
Disease:
Spinocerebellar ataxia 14
C 0.700 CausalMutation CLINVAR
dbSNP: rs386134160
rs386134160
Entrez Id: 5582
Gene Symbol: PRKCG
PRKCG
CUI: C1854369
Disease:
Spinocerebellar ataxia 14
A 0.700 CausalMutation CLINVAR
dbSNP: rs386134161
rs386134161
Entrez Id: 5582
Gene Symbol: PRKCG
PRKCG
CUI: C1854369
Disease:
Spinocerebellar ataxia 14
A 0.700 CausalMutation CLINVAR
dbSNP: rs386134162
rs386134162
Entrez Id: 5582
Gene Symbol: PRKCG
PRKCG
CUI: C1854369
Disease:
Spinocerebellar ataxia 14
A 0.700 CausalMutation CLINVAR
dbSNP: rs386134163
rs386134163
Entrez Id: 5582
Gene Symbol: PRKCG
PRKCG
CUI: C1854369
Disease:
Spinocerebellar ataxia 14
T 0.700 CausalMutation CLINVAR
dbSNP: rs386134164
rs386134164
Entrez Id: 5582
Gene Symbol: PRKCG
PRKCG
CUI: C1854369
Disease:
Spinocerebellar ataxia 14
A 0.700 CausalMutation CLINVAR
dbSNP: rs386134165
rs386134165
Entrez Id: 5582
Gene Symbol: PRKCG
PRKCG
CUI: C1854369
Disease:
Spinocerebellar ataxia 14
A 0.700 CausalMutation CLINVAR
dbSNP: rs386134166
rs386134166
Entrez Id: 5582
Gene Symbol: PRKCG
PRKCG
CUI: C1854369
Disease:
Spinocerebellar ataxia 14
C 0.700 CausalMutation CLINVAR
dbSNP: rs386134167
rs386134167
Entrez Id: 5582
Gene Symbol: PRKCG
PRKCG
CUI: C1854369
Disease:
Spinocerebellar ataxia 14
A 0.700 CausalMutation CLINVAR
dbSNP: rs386134169
rs386134169
Entrez Id: 5582
Gene Symbol: PRKCG
PRKCG
CUI: C1854369
Disease:
Spinocerebellar ataxia 14
A 0.700 CausalMutation CLINVAR
dbSNP: rs386134170
rs386134170
Entrez Id: 5582
Gene Symbol: PRKCG
PRKCG
CUI: C1854369
Disease:
Spinocerebellar ataxia 14
TT 0.700 CausalMutation CLINVAR
dbSNP: rs386134171
rs386134171
Entrez Id: 5582
Gene Symbol: PRKCG
PRKCG
CUI: C1854369
Disease:
Spinocerebellar ataxia 14
A 0.700 CausalMutation CLINVAR