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: rs2786098
rs2786098
1.000 0.080 1 197356778 intron variant T/A;G snv
CUI: C0004096
Disease: Asthma
Asthma
0.810 1.000 1 2010 2010
dbSNP: rs10754220
rs10754220
1 197275160 intron variant G/A snv 0.22
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 2 2017 2018
dbSNP: rs1009188
rs1009188
1 197287960 intron variant T/C snv 0.22
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2019 2019
dbSNP: rs12042924
rs12042924
1 197328287 intron variant T/C snv 0.41
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure
0.700 1.000 1 2018 2018
dbSNP: rs2759663
rs2759663
0.925 0.080 1 197415296 intron variant C/G;T snv
CUI: C0149745
Disease: Oral Ulcer
Oral Ulcer
0.700 1.000 1 2019 2019
dbSNP: rs2759663
rs2759663
0.925 0.080 1 197415296 intron variant C/G;T snv
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder
0.700 1.000 1 2018 2018
dbSNP: rs2786107
rs2786107
1 197341647 intron variant G/T snv 0.80
CUI: C0523688
Disease: Hemopexin measurement
Hemopexin measurement
0.700 1.000 1 2017 2017
dbSNP: rs6689858
rs6689858
0.724 0.240 1 197406337 intron variant T/C snv 0.39
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
0.700 1.000 1 2015 2015
dbSNP: rs6689858
rs6689858
0.724 0.240 1 197406337 intron variant T/C snv 0.39
Diabetes Mellitus, Insulin-Dependent
0.700 1.000 1 2015 2015
dbSNP: rs6689858
rs6689858
0.724 0.240 1 197406337 intron variant T/C snv 0.39
CUI: C0007570
Disease: Celiac Disease
Celiac Disease
0.700 1.000 1 2015 2015
dbSNP: rs6689858
rs6689858
0.724 0.240 1 197406337 intron variant T/C snv 0.39
CUI: C0033860
Disease: Psoriasis
Psoriasis
0.700 1.000 1 2015 2015
dbSNP: rs6689858
rs6689858
0.724 0.240 1 197406337 intron variant T/C snv 0.39
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases
0.700 1.000 1 2015 2015
dbSNP: rs6689858
rs6689858
0.724 0.240 1 197406337 intron variant T/C snv 0.39
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 1.000 1 2015 2015
dbSNP: rs6689858
rs6689858
0.724 0.240 1 197406337 intron variant T/C snv 0.39
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2
0.700 1.000 1 2015 2015
dbSNP: rs6689858
rs6689858
0.724 0.240 1 197406337 intron variant T/C snv 0.39
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
0.700 1.000 1 2015 2015
dbSNP: rs6689858
rs6689858
0.724 0.240 1 197406337 intron variant T/C snv 0.39
CUI: C0920350
Disease: Autoimmune thyroiditis
Autoimmune thyroiditis
0.700 1.000 1 2015 2015
dbSNP: rs6689858
rs6689858
0.724 0.240 1 197406337 intron variant T/C snv 0.39
AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6
0.700 1.000 1 2015 2015
dbSNP: rs6689858
rs6689858
0.724 0.240 1 197406337 intron variant T/C snv 0.39
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1
0.700 1.000 1 2015 2015
dbSNP: rs6689858
rs6689858
0.724 0.240 1 197406337 intron variant T/C snv 0.39
CUI: C3495559
Disease: Juvenile arthritis
Juvenile arthritis
0.700 1.000 1 2015 2015
dbSNP: rs6689858
rs6689858
0.724 0.240 1 197406337 intron variant T/C snv 0.39
CUI: C0009447
Disease: Common Variable Immunodeficiency
Common Variable Immunodeficiency
0.700 1.000 1 2015 2015
dbSNP: rs6689858
rs6689858
0.724 0.240 1 197406337 intron variant T/C snv 0.39
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis
0.700 1.000 1 2015 2015
dbSNP: rs76169311
rs76169311
1.000 0.120 1 197372771 intron variant G/A snv 0.13
CUI: C0202123
Disease: Luteinizing hormone measurement
Luteinizing hormone measurement
0.700 1.000 1 2015 2015
dbSNP: rs76169311
rs76169311
1.000 0.120 1 197372771 intron variant G/A snv 0.13
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome
0.700 1.000 1 2015 2015