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: rs12506688
rs12506688
1.000 0.120 4 26102491 intron variant C/T snv 0.27
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.800 1.000 2 2012 2015
dbSNP: rs10517086
rs10517086
0.882 0.160 4 26083889 intron variant G/A snv 0.27
Diabetes Mellitus, Insulin-Dependent
0.800 1.000 1 2009 2009
dbSNP: rs17630466
rs17630466
1.000 0.120 4 26084947 intron variant A/G snv 0.28
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.800 1.000 1 2012 2012
dbSNP: rs2137234
rs2137234
4 26078927 intron variant T/C snv 0.30
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio
0.700 1.000 1 2019 2019
dbSNP: rs6448432
rs6448432
1.000 0.120 4 26097188 intron variant G/A;T snv
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.700 1.000 1 2014 2014
dbSNP: rs7441808
rs7441808
0.851 0.040 4 26088753 intron variant A/G snv 0.20
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1
0.700 1.000 1 2019 2019
dbSNP: rs7441808
rs7441808
0.851 0.040 4 26088753 intron variant A/G snv 0.20
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2
0.700 1.000 1 2019 2019
dbSNP: rs7441808
rs7441808
0.851 0.040 4 26088753 intron variant A/G snv 0.20
AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6
0.700 1.000 1 2019 2019
dbSNP: rs7441808
rs7441808
0.851 0.040 4 26088753 intron variant A/G snv 0.20
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism
0.700 1.000 1 2019 2019
dbSNP: rs7441808
rs7441808
0.851 0.040 4 26088753 intron variant A/G snv 0.20
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases
0.700 1.000 1 2019 2019
dbSNP: rs932036
rs932036
1.000 0.120 4 26089240 intron variant A/G;T snv
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2019 2019