Source: GWASDB

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: rs10486483
rs10486483
1.000 0.040 7 26852821 intron variant G/A snv 0.21
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.800 1.000 1 2012 2015
dbSNP: rs7804356
rs7804356
0.925 0.160 7 26852046 intron variant T/C snv 0.21
Diabetes Mellitus, Insulin-Dependent
0.800 1.000 1 2009 2009
dbSNP: rs7804356
rs7804356
0.925 0.160 7 26852046 intron variant T/C snv 0.21
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.700 1.000 1 2011 2011