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: rs6545800
rs6545800
2 24896016 intron variant C/T snv 0.53
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.800 1.000 1 2012 2012
dbSNP: rs6545814
rs6545814
2 24908447 intron variant A/G snv 0.53
CUI: C0578022
Disease: Finding of body mass index
Finding of body mass index
0.700 1.000 2 2012 2014
dbSNP: rs6545814
rs6545814
2 24908447 intron variant A/G snv 0.53
CUI: C0005893
Disease: Body mass index procedure
Body mass index procedure
0.700 1.000 2 2012 2014
dbSNP: rs11676272
rs11676272
1.000 0.040 2 24918669 missense variant A/G snv 0.47 0.57
CUI: C0005893
Disease: Body mass index procedure
Body mass index procedure
0.700 1.000 1 2012 2012
dbSNP: rs11676272
rs11676272
1.000 0.040 2 24918669 missense variant A/G snv 0.47 0.57
CUI: C0578022
Disease: Finding of body mass index
Finding of body mass index
0.700 1.000 1 2012 2012
dbSNP: rs7586879
rs7586879
2 24894108 intron variant C/T snv 0.47
CUI: C0578022
Disease: Finding of body mass index
Finding of body mass index
0.700 1.000 1 2013 2013
dbSNP: rs7586879
rs7586879
2 24894108 intron variant C/T snv 0.47
CUI: C0005893
Disease: Body mass index procedure
Body mass index procedure
0.700 1.000 1 2013 2013