Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs17669
rs17669
MIR122 ; MIR3591
0.851 0.160 18 58451261 non coding transcript exon variant C/A;T snv 0.72
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke 		0.020 0.500 2 2019 2020
dbSNP: rs17669
rs17669
MIR122 ; MIR3591
0.851 0.160 18 58451261 non coding transcript exon variant C/A;T snv 0.72
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident 		0.010 1.000 1 2020 2020
dbSNP: rs17669
rs17669
MIR122 ; MIR3591
0.851 0.160 18 58451261 non coding transcript exon variant C/A;T snv 0.72
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		0.010 1.000 1 2018 2018
dbSNP: rs17669
rs17669
MIR122 ; MIR3591
0.851 0.160 18 58451261 non coding transcript exon variant C/A;T snv 0.72
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.010 1.000 1 2017 2017
dbSNP: rs17669
rs17669
MIR122 ; MIR3591
0.851 0.160 18 58451261 non coding transcript exon variant C/A;T snv 0.72
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.010 1.000 1 2017 2017