Source: GWASCAT

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: rs2119704
rs2119704
LINC01147
1.000 0.080 14 88021345 intron variant C/A snv 0.11
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.800 1.000 1 2011 2011
dbSNP: rs11624293
rs11624293
LINC01147
0.827 0.120 14 88022477 intron variant T/C snv 0.13
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		0.710 1.000 2 2013 2019
dbSNP: rs11624293
rs11624293
LINC01147
0.827 0.120 14 88022477 intron variant T/C snv 0.13
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 1.000 1 2016 2016
dbSNP: rs11624293
rs11624293
LINC01147
0.827 0.120 14 88022477 intron variant T/C snv 0.13
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.700 1.000 1 2016 2016
dbSNP: rs11624293
rs11624293
LINC01147
0.827 0.120 14 88022477 intron variant T/C snv 0.13
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.700 1.000 1 2016 2016
dbSNP: rs11624293
rs11624293
LINC01147
0.827 0.120 14 88022477 intron variant T/C snv 0.13
CUI: C0008313
Disease: Cholangitis, Sclerosing
Cholangitis, Sclerosing 		0.700 1.000 1 2016 2016