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: rs2287019
rs2287019
7 1.000 0.080 19 45698914 intron variant C/T snv 0.17 0.16 0.700 1.000 2 2015 2019
dbSNP: rs2765539
rs2765539
1 1 119006795 TF binding site variant C/G;T snv 0.700 1.000 2 2015 2019
dbSNP: rs4929927
rs4929927
1 11 8636938 intron variant A/G;T snv 0.700 1.000 2 2015 2019
dbSNP: rs7801581
rs7801581
5 7 27184152 intron variant C/T snv 0.24 0.700 1.000 2 2015 2018
dbSNP: rs863750
rs863750
7 12 124020897 intron variant C/T snv 0.53 0.700 1.000 2 2015 2019
dbSNP: rs929641
rs929641
3 2 58565242 intron variant A/G snv 0.45 0.700 1.000 2 2015 2019
dbSNP: rs10245353
rs10245353
4 7 25818994 intergenic variant C/A snv 0.16 0.700 1.000 1 2015 2015
dbSNP: rs10804591
rs10804591
5 3 129615390 intergenic variant C/A snv 0.63 0.700 1.000 1 2015 2015
dbSNP: rs11048470
rs11048470
1 12 26334350 intron variant G/T snv 0.26 0.700 1.000 1 2015 2015
dbSNP: rs1121980
rs1121980
FTO
18 0.807 0.240 16 53775335 intron variant G/A;C snv 0.700 1.000 1 2015 2015
dbSNP: rs11663816
rs11663816
4 18 60208994 intergenic variant T/C snv 0.20 0.700 1.000 1 2015 2015
dbSNP: rs11989744
rs11989744
1 8 23709950 intron variant C/T snv 0.25 0.700 1.000 1 2015 2015
dbSNP: rs12549058
rs12549058
1 8 71580003 intron variant T/A;G snv 0.700 1.000 1 2015 2015
dbSNP: rs1394461
rs1394461
1 11 99351618 intron variant G/C snv 0.21 0.700 1.000 1 2015 2015
dbSNP: rs1515108
rs1515108
1 2 226258370 intergenic variant C/T snv 0.60 0.700 1.000 1 2015 2015
dbSNP: rs16996700
rs16996700
3 20 52365406 intron variant T/C snv 0.29 0.700 1.000 1 2015 2015
dbSNP: rs2075650
rs2075650
45 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 0.700 1.000 1 2015 2015
dbSNP: rs2179129
rs2179129
2 22 29054935 3 prime UTR variant A/G snv 0.34 0.700 1.000 1 2015 2015
dbSNP: rs319564
rs319564
1 13 93180626 intergenic variant C/T snv 0.45 0.700 1.000 1 2015 2015
dbSNP: rs4471313
rs4471313
1 1 170398325 intergenic variant G/A;T snv 0.700 1.000 1 2015 2015
dbSNP: rs4640244
rs4640244
3 17 21380911 intron variant A/G snv 0.33 0.700 1.000 1 2015 2015
dbSNP: rs4646404
rs4646404
1 17 17516885 intron variant G/A snv 0.24 0.700 1.000 1 2015 2015
dbSNP: rs4715208
rs4715208
1 6 50861758 upstream gene variant A/C;G;T snv 0.700 1.000 1 2015 2015
dbSNP: rs4846565
rs4846565
2 1 219548762 intergenic variant G/A snv 0.26 0.700 1.000 1 2015 2015
dbSNP: rs9860730
rs9860730
3 3 64715470 intron variant A/G snv 0.50 0.700 1.000 1 2015 2015