IFT172, intraflagellar transport 172, 26160

N. diseases: 123; N. variants: 31
Disease: RETINITIS PIGMENTOSA 71 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs786205855
rs786205855
Entrez Id: 26160;200634
Gene Symbol: IFT172;KRTCAP3
IFT172;KRTCAP3
CUI: C4225342
Disease:
RETINITIS PIGMENTOSA 71 		T 0.800 CausalMutation CLINVAR
dbSNP: rs786205855
rs786205855
Entrez Id: 26160;200634
Gene Symbol: IFT172;KRTCAP3
IFT172;KRTCAP3
CUI: C4225342
Disease:
RETINITIS PIGMENTOSA 71 		0.800 GeneticVariation UNIPROT
dbSNP: rs786205856
rs786205856
Entrez Id: 26160;200634
Gene Symbol: IFT172;KRTCAP3
IFT172;KRTCAP3
CUI: C4225342
Disease:
RETINITIS PIGMENTOSA 71 		C 0.800 CausalMutation CLINVAR
dbSNP: rs786205856
rs786205856
Entrez Id: 26160;200634
Gene Symbol: IFT172;KRTCAP3
IFT172;KRTCAP3
CUI: C4225342
Disease:
RETINITIS PIGMENTOSA 71 		0.800 GeneticVariation UNIPROT
dbSNP: rs786205857
rs786205857
Entrez Id: 26160
Gene Symbol: IFT172
IFT172
CUI: C4225342
Disease:
RETINITIS PIGMENTOSA 71 		0.800 GeneticVariation UNIPROT
dbSNP: rs786205857
rs786205857
Entrez Id: 26160
Gene Symbol: IFT172
IFT172
CUI: C4225342
Disease:
RETINITIS PIGMENTOSA 71 		G 0.800 CausalMutation CLINVAR
dbSNP: rs1250676888
rs1250676888
Entrez Id: 26160
Gene Symbol: IFT172
IFT172
CUI: C4225342
Disease:
RETINITIS PIGMENTOSA 71 		A 0.700 CausalMutation CLINVAR
dbSNP: rs370540673
rs370540673
Entrez Id: 26160
Gene Symbol: IFT172
IFT172
CUI: C4225342
Disease:
RETINITIS PIGMENTOSA 71 		T 0.700 CausalMutation CLINVAR
dbSNP: rs750338419
rs750338419
Entrez Id: 26160
Gene Symbol: IFT172
IFT172
CUI: C4225342
Disease:
RETINITIS PIGMENTOSA 71 		AT 0.700 CausalMutation CLINVAR
dbSNP: rs786205858
rs786205858
Entrez Id: 26160
Gene Symbol: IFT172
IFT172
CUI: C4225342
Disease:
RETINITIS PIGMENTOSA 71 		T 0.700 CausalMutation CLINVAR