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: rs10734411
rs10734411
1 11 32520238 intergenic variant G/A snv 0.56 0.700 1.000 2 2015 2019
dbSNP: rs2384687
rs2384687
1 19 55319820 non coding transcript exon variant A/G snv 0.38 0.700 1.000 2 2009 2013
dbSNP: rs349306
rs349306
1 19 950694 intron variant G/A snv 0.87 0.700 1.000 2 2015 2019
dbSNP: rs75770066
rs75770066
1 12 66310445 missense variant A/G snv 3.1E-02 2.5E-02 0.700 1.000 2 2015 2019
dbSNP: rs897798
rs897798
1 19 55322386 intron variant A/G snv 0.46 0.700 1.000 2 2009 2013
dbSNP: rs10049761
rs10049761
1 4 48684940 intron variant G/T snv 0.51 0.700 1.000 1 2018 2018
dbSNP: rs10145469
rs10145469
1 14 97303497 intergenic variant C/A snv 5.7E-02 0.700 1.000 1 2018 2018
dbSNP: rs10156597
rs10156597
2 9 106179228 intron variant A/T snv 0.36 0.700 1.000 1 2018 2018
dbSNP: rs1029285
rs1029285
1 16 11893261 intron variant G/A snv 0.43 0.700 1.000 1 2019 2019
dbSNP: rs10521305
rs10521305
FTO
1 16 53874572 intron variant T/C snv 4.4E-02 0.700 1.000 1 2019 2019
dbSNP: rs1054875
rs1054875
1 15 89335895 non coding transcript exon variant A/G;T snv 0.700 1.000 1 2015 2015
dbSNP: rs10813912
rs10813912
1 9 32975212 non coding transcript exon variant A/G snv 0.62 0.700 1.000 1 2019 2019
dbSNP: rs10840614
rs10840614
1 12 121753584 intron variant A/C snv 0.50 0.700 1.000 1 2019 2019
dbSNP: rs10854167
rs10854167
1 20 62901687 intron variant G/C snv 0.18 0.700 1.000 1 2019 2019
dbSNP: rs10905065
rs10905065
1 10 5727864 intron variant G/A snv 0.53 0.700 1.000 1 2015 2015
dbSNP: rs10931831
rs10931831
1 2 198756917 intron variant C/T snv 0.43 0.700 1.000 1 2018 2018
dbSNP: rs10934420
rs10934420
1 3 117833264 intron variant T/C snv 0.44 0.700 1.000 1 2018 2018
dbSNP: rs10937153
rs10937153
1 3 183845137 intron variant G/A snv 0.27 0.700 1.000 1 2019 2019
dbSNP: rs10957156
rs10957156
1 8 60716842 intron variant G/A snv 0.77 0.700 1.000 1 2015 2015
dbSNP: rs10998203
rs10998203
1 10 68464775 intron variant C/G snv 0.31 0.700 1.000 1 2019 2019
dbSNP: rs11031005
rs11031005
5 1.000 0.120 11 30204809 intron variant T/C snv 0.10 0.700 1.000 1 2019 2019
dbSNP: rs11031006
rs11031006
8 0.882 0.120 11 30204981 intron variant G/A snv 0.11 0.700 1.000 1 2015 2015
dbSNP: rs11070328
rs11070328
1 15 41359371 intron variant T/C snv 0.21 0.700 1.000 1 2012 2012
dbSNP: rs11180609
rs11180609
1 12 75646612 intron variant T/C snv 0.10 0.700 1.000 1 2019 2019
dbSNP: rs11195485
rs11195485
1 10 111244059 intergenic variant C/T snv 4.2E-03 0.700 1.000 1 2013 2013