Source: GWASDB ×
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs10168266
rs10168266
STAT4
3 0.776 0.400 2 191071078 intron variant C/T snv 0.19 0.800 1.000 1 2013 2013
dbSNP: rs117026326
rs117026326
GTF2I ; LOC101926943
1 0.752 0.440 7 74711703 intron variant C/T snv 1.3E-02 0.800 1.000 1 2013 2016
dbSNP: rs4282438
rs4282438
COL11A2P1
2 0.807 0.280 6 33104395 intron variant T/G snv 3.1E-02 0.800 1.000 1 2013 2013
dbSNP: rs5029939
rs5029939
TNFAIP3
2 0.701 0.440 6 137874586 intron variant C/G snv 0.13 0.800 1.000 1 2013 2013
dbSNP: rs9271588
rs9271588 		1 0.925 0.200 6 32623176 TF binding site variant T/C snv 0.43 0.800 1.000 1 2013 2013