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: rs12352785
rs12352785
9 6956850 intron variant A/C snv 0.74
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2018 2018
dbSNP: rs12984770
rs12984770
19 18356588 intron variant A/C snv 0.23
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2019 2019
dbSNP: rs13263601
rs13263601
8 14238391 intron variant A/C snv 0.28
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2019 2019
dbSNP: rs13292699
rs13292699
9 15910046 intron variant A/C snv 0.34
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2019 2019
dbSNP: rs13396415
rs13396415
2 142074189 intron variant A/C snv 0.18
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2019 2019
dbSNP: rs1394877
rs1394877
13 62110317 regulatory region variant A/C snv 0.39
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2019 2019
dbSNP: rs1411432
rs1411432
9 16728534 intron variant A/C snv 0.19
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2019 2019
dbSNP: rs1470579
rs1470579
0.925 0.160 3 185811292 intron variant A/C snv 0.46
CUI: C1305855
Disease: Body mass index
Body mass index
0.800 1.000 1 2012 2012
dbSNP: rs1536166
rs1536166
1 83961369 intron variant A/C snv 0.25
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2019 2019
dbSNP: rs1555543
rs1555543
1 96479241 intergenic variant A/C snv 0.55
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2010 2010
dbSNP: rs181179291
rs181179291
16 2737061 downstream gene variant A/C snv 7.0E-03
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2019 2019
dbSNP: rs185581
rs185581
2 59653470 intron variant A/C snv 0.84
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2019 2019
dbSNP: rs1933440
rs1933440
13 28102834 upstream gene variant A/C snv 0.13
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2019 2019
dbSNP: rs2105808
rs2105808
11 132770106 intron variant A/C snv 0.26
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2019 2019
dbSNP: rs2239647
rs2239647
0.851 0.080 14 32823537 synonymous variant A/C snv 0.60 0.65
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2019 2019
dbSNP: rs2390669
rs2390669
1.000 0.040 2 168235432 intron variant A/C snv 0.14
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2017 2017
dbSNP: rs2425840
rs2425840
20 46276199 intron variant A/C snv 0.32
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2019 2019
dbSNP: rs2528531
rs2528531
7 93607198 intron variant A/C snv 0.31
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2019 2019
dbSNP: rs2546057
rs2546057
1.000 0.040 19 33829949 intergenic variant A/C snv 0.41
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2017 2017
dbSNP: rs2583410
rs2583410
4 101261042 intron variant A/C snv 0.19
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2019 2019
dbSNP: rs2606228
rs2606228
3 183819971 intron variant A/C snv 0.75
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2019 2019
dbSNP: rs2980853
rs2980853
0.851 0.120 8 125466108 upstream gene variant A/C snv 0.43
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2016 2016
dbSNP: rs3125326
rs3125326
10 61294030 intergenic variant A/C snv 0.60
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2019 2019
dbSNP: rs3736594
rs3736594
2 27772914 intron variant A/C snv 0.62
CUI: C1305855
Disease: Body mass index
Body mass index
0.800 1.000 1 2012 2012
dbSNP: rs3778934
rs3778934
7 39405786 intron variant A/C snv 0.34
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2019 2019