SLC24A1, solute carrier family 24 member 1, 9187

N. diseases: 28; N. variants: 13
Disease: NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1D ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1410075831
rs1410075831
Entrez Id: 9187
Gene Symbol: SLC24A1
SLC24A1
CUI: C3151193
Disease:
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1D 		T 0.700 CausalMutation CLINVAR
dbSNP: rs1555403793
rs1555403793
Entrez Id: 9187
Gene Symbol: SLC24A1
SLC24A1
CUI: C3151193
Disease:
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1D 		C 0.700 CausalMutation CLINVAR
dbSNP: rs1555407654
rs1555407654
Entrez Id: 9187
Gene Symbol: SLC24A1
SLC24A1
CUI: C3151193
Disease:
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1D 		C 0.700 CausalMutation CLINVAR
dbSNP: rs766780281
rs766780281
Entrez Id: 9187
Gene Symbol: SLC24A1
SLC24A1
CUI: C3151193
Disease:
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1D 		G 0.700 CausalMutation CLINVAR
dbSNP: rs777989874
rs777989874
Entrez Id: 9187
Gene Symbol: SLC24A1
SLC24A1
CUI: C3151193
Disease:
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1D 		A 0.700 CausalMutation CLINVAR