PROM1, prominin 1, 8842

N. diseases: 477; N. variants: 33
Disease: RETINITIS PIGMENTOSA 41 (disorder) ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs137853005
rs137853005
Entrez Id: 8842
Gene Symbol: PROM1
PROM1
CUI: C2677516
Disease:
RETINITIS PIGMENTOSA 41 (disorder) 		A 0.700 CausalMutation CLINVAR
dbSNP: rs530749007
rs530749007
Entrez Id: 8842
Gene Symbol: PROM1
PROM1
CUI: C2677516
Disease:
RETINITIS PIGMENTOSA 41 (disorder) 		A 0.700 CausalMutation CLINVAR
dbSNP: rs543698823
rs543698823
Entrez Id: 8842
Gene Symbol: PROM1
PROM1
CUI: C2677516
Disease:
RETINITIS PIGMENTOSA 41 (disorder) 		TA 0.700 CausalMutation CLINVAR
dbSNP: rs746174328
rs746174328
Entrez Id: 8842
Gene Symbol: PROM1
PROM1
CUI: C2677516
Disease:
RETINITIS PIGMENTOSA 41 (disorder) 		G 0.700 CausalMutation CLINVAR
dbSNP: rs766246531
rs766246531
Entrez Id: 8842
Gene Symbol: PROM1
PROM1
CUI: C2677516
Disease:
RETINITIS PIGMENTOSA 41 (disorder) 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs780697796
rs780697796
Entrez Id: 8842
Gene Symbol: PROM1
PROM1
CUI: C2677516
Disease:
RETINITIS PIGMENTOSA 41 (disorder) 		A 0.700 CausalMutation CLINVAR
dbSNP: rs886037612
rs886037612
Entrez Id: 8842
Gene Symbol: PROM1
PROM1
CUI: C2677516
Disease:
RETINITIS PIGMENTOSA 41 (disorder) 		T 0.700 CausalMutation CLINVAR