Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs6780013
rs6780013
Entrez Id: 25930
Gene Symbol: PTPN23
PTPN23
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent
G 0.700 GeneticVariation GWASCAT Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes. 29632382 2018
dbSNP: rs138076291
rs138076291
Entrez Id: 25930
Gene Symbol: PTPN23
PTPN23
CUI: C4551584
Disease:
Brain atrophy
T 0.700 GeneticVariation CLINVAR
dbSNP: rs138076291
rs138076291
Entrez Id: 25930
Gene Symbol: PTPN23
PTPN23
CUI: C0557874
Disease:
Global developmental delay
T 0.700 GeneticVariation CLINVAR
dbSNP: rs147293860
rs147293860
Entrez Id: 25930
Gene Symbol: PTPN23
PTPN23
CUI: C0557874
Disease:
Global developmental delay
G 0.700 GeneticVariation CLINVAR
dbSNP: rs147293860
rs147293860
Entrez Id: 25930
Gene Symbol: PTPN23
PTPN23
CUI: C4551584
Disease:
Brain atrophy
G 0.700 GeneticVariation CLINVAR
dbSNP: rs150712932
rs150712932
Entrez Id: 25930
Gene Symbol: PTPN23
PTPN23
CUI: C0557874
Disease:
Global developmental delay
T 0.700 GeneticVariation CLINVAR
dbSNP: rs150712932
rs150712932
Entrez Id: 25930
Gene Symbol: PTPN23
PTPN23
CUI: C4551584
Disease:
Brain atrophy
T 0.700 GeneticVariation CLINVAR
dbSNP: rs577689618
rs577689618
Entrez Id: 25930
Gene Symbol: PTPN23
PTPN23
CUI: C4551584
Disease:
Brain atrophy
A 0.700 GeneticVariation CLINVAR
dbSNP: rs577689618
rs577689618
Entrez Id: 25930
Gene Symbol: PTPN23
PTPN23
CUI: C0557874
Disease:
Global developmental delay
A 0.700 GeneticVariation CLINVAR
dbSNP: rs730882229
rs730882229
Entrez Id: 25930
Gene Symbol: PTPN23
PTPN23
CUI: C0014544
Disease:
Epilepsy
T 0.700 GeneticVariation CLINVAR
dbSNP: rs730882229
rs730882229
Entrez Id: 25930
Gene Symbol: PTPN23
PTPN23
CUI: C4551584
Disease:
Brain atrophy
T 0.700 GeneticVariation CLINVAR
dbSNP: rs730882229
rs730882229
Entrez Id: 25930
Gene Symbol: PTPN23
PTPN23
CUI: C0557874
Disease:
Global developmental delay
T 0.700 GeneticVariation CLINVAR
dbSNP: rs770692989
rs770692989
Entrez Id: 25930
Gene Symbol: PTPN23
PTPN23
CUI: C0557874
Disease:
Global developmental delay
G 0.700 GeneticVariation CLINVAR
dbSNP: rs770692989
rs770692989
Entrez Id: 25930
Gene Symbol: PTPN23
PTPN23
CUI: C4551584
Disease:
Brain atrophy
G 0.700 GeneticVariation CLINVAR
dbSNP: rs967738491
rs967738491
Entrez Id: 25930
Gene Symbol: PTPN23
PTPN23
CUI: C4551584
Disease:
Brain atrophy
T 0.700 GeneticVariation CLINVAR
dbSNP: rs967738491
rs967738491
Entrez Id: 25930
Gene Symbol: PTPN23
PTPN23
CUI: C0557874
Disease:
Global developmental delay
T 0.700 GeneticVariation CLINVAR