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: rs17535749
rs17535749
EMC3 ; EMC3-AS1
3 9986040 intron variant G/A snv 7.2E-02
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs11761528
rs11761528
ZKSCAN5
1.000 0.120 7 99521178 intron variant C/T snv 0.12
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs3901286
rs3901286
ZKSCAN5
7 99510104 intron variant C/A snv 0.38
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs6707827
rs6707827 		2 99506568 intergenic variant A/G snv 0.79
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs12551906
rs12551906
NAMA
9 99356808 intron variant G/A snv 0.21
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs1229984
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 2 2017 2019
dbSNP: rs10760678
rs10760678 		9 99317659 intergenic variant G/A snv 0.34
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs923724
rs923724
ANKS1B
12 99246152 intron variant G/C snv 0.55
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs4082793
rs4082793
BCL11B
14 99233743 intron variant C/T snv 0.30
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs2693686
rs2693686
BCL11B
14 99206460 intron variant C/G snv 0.42
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs2372716
rs2372716
ANKS1B
12 99179648 intron variant C/T snv 0.84
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2018 2018
dbSNP: rs651548
rs651548
ANKS1B
12 99166405 intron variant A/G snv 0.54
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs660879
rs660879
ANKS1B
12 99160037 intron variant T/A;C;G snv
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs34303684
rs34303684
PGPEP1L
15 98976030 intron variant G/A;C snv
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs325220
rs325220
LINC02062
5 98968860 intron variant G/A snv 0.28
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs2715423
rs2715423
PGPEP1L
15 98968644 missense variant G/A snv 0.23 0.21
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs150992
rs150992
LINC02062
5 98939493 intron variant A/G snv 0.29
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2015 2015
dbSNP: rs17150703
rs17150703 		1.000 0.080 8 9888288 intergenic variant G/A snv 8.5E-02
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs12227147
rs12227147
ANKS1B
12 98849243 intron variant T/A snv 1.9E-02
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2018 2018
dbSNP: rs580809
rs580809
ANKS6
9 98756160 intron variant C/T snv 0.78
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2017 2017
dbSNP: rs58139454
rs58139454
IGF1R
15 98686933 intron variant G/C snv 0.18
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs56803094
rs56803094
IGF1R
15 98679280 intron variant A/G snv 0.19
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs7334078
rs7334078
STK24
13 98468230 intron variant T/C snv 0.29
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs17574378
rs17574378
STK24
13 98464130 intron variant T/C snv 0.29
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs1983864
rs1983864
LOXL4
10 98257696 missense variant T/G snv 0.39 0.29
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2018 2018