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: rs4561177
rs4561177
RDX ; ZC3H12C
0.807 0.120 11 110091706 intron variant A/G snv 0.36
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.800 1.000 2 2012 2016
dbSNP: rs10789752
rs10789752
RDX ; ZC3H12C
11 110109220 intron variant T/A;C snv
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2018 2018
dbSNP: rs4561177
rs4561177
RDX ; ZC3H12C
0.807 0.120 11 110091706 intron variant A/G snv 0.36
CUI: C0008313
Disease: Cholangitis, Sclerosing
Cholangitis, Sclerosing 		0.700 1.000 1 2016 2016
dbSNP: rs4561177
rs4561177
RDX ; ZC3H12C
0.807 0.120 11 110091706 intron variant A/G snv 0.36
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 1.000 1 2016 2016
dbSNP: rs4561177
rs4561177
RDX ; ZC3H12C
0.807 0.120 11 110091706 intron variant A/G snv 0.36
CUI: C0263361
Disease: Psoriasis vulgaris
Psoriasis vulgaris 		0.700 1.000 1 2015 2015
dbSNP: rs4561177
rs4561177
RDX ; ZC3H12C
0.807 0.120 11 110091706 intron variant A/G snv 0.36
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		0.700 1.000 1 2016 2016
dbSNP: rs4561177
rs4561177
RDX ; ZC3H12C
0.807 0.120 11 110091706 intron variant A/G snv 0.36
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.700 1.000 1 2016 2016
dbSNP: rs661171
rs661171
RDX ; ZC3H12C
11 110145794 intron variant T/G snv 0.69
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2018 2018
dbSNP: rs661171
rs661171
RDX ; ZC3H12C
11 110145794 intron variant T/G snv 0.69
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2018 2018
dbSNP: rs661171
rs661171
RDX ; ZC3H12C
11 110145794 intron variant T/G snv 0.69
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2018 2018
dbSNP: rs661171
rs661171
RDX ; ZC3H12C
11 110145794 intron variant T/G snv 0.69
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2018 2018
dbSNP: rs661171
rs661171
RDX ; ZC3H12C
11 110145794 intron variant T/G snv 0.69
CUI: C0202159
Disease: Parathyroid hormone measurement
Parathyroid hormone measurement 		0.700 1.000 1 2018 2018
dbSNP: rs689183
rs689183
RDX ; ZC3H12C
11 110141418 intron variant G/T snv 0.74
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2018 2018
dbSNP: rs746463
rs746463
RDX ; ZC3H12C
11 110125219 intron variant C/T snv 0.71
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2017 2017