Source: ALL
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: rs4471028
rs4471028
GDAP1
1 8 74382740 intron variant T/G snv 0.36 0.800 1.000 1 2007 2007
dbSNP: rs12970134
rs12970134 		13 0.790 0.280 18 60217517 intergenic variant G/A snv 0.21 0.700 1.000 1 2008 2008
dbSNP: rs1558902
rs1558902
FTO
21 0.827 0.120 16 53769662 intron variant T/A snv 0.31 0.800 1.000 3 2009 2017
dbSNP: rs11152213
rs11152213 		4 1.000 0.080 18 60185715 intergenic variant A/C;T snv 0.800 1.000 2 2009 2019
dbSNP: rs12967135
rs12967135 		8 18 60181790 intergenic variant G/A snv 0.24 0.800 1.000 2 2009 2017
dbSNP: rs1421085
rs1421085
FTO
28 0.752 0.280 16 53767042 intron variant T/C snv 0.31 0.800 1.000 2 2009 2019
dbSNP: rs6567160
rs6567160 		12 1.000 0.080 18 60161902 upstream gene variant T/C snv 0.21 0.800 1.000 2 2009 2015
dbSNP: rs7138803
rs7138803 		17 0.827 0.240 12 49853685 intergenic variant G/A;T snv 0.800 1.000 2 2009 2015
dbSNP: rs7144011
rs7144011
NRXN3
4 1.000 0.080 14 79474040 intron variant G/T snv 0.21 0.800 1.000 2 2009 2015
dbSNP: rs10145154
rs10145154
NRXN3
1 14 79473182 intron variant C/T snv 0.25 0.700 1.000 1 2009 2009
dbSNP: rs10146997
rs10146997
NRXN3
6 0.827 0.240 14 79478819 intron variant A/G snv 0.25 0.800 1.000 1 2009 2009
dbSNP: rs10150332
rs10150332
NRXN3
4 14 79470621 intron variant T/C snv 0.26 0.700 1.000 1 2009 2009
dbSNP: rs10852521
rs10852521
FTO
2 1.000 0.080 16 53771053 intron variant T/A;C snv 0.700 1.000 1 2009 2009
dbSNP: rs10871777
rs10871777 		6 0.925 0.120 18 60184530 intergenic variant A/G snv 0.24 0.700 1.000 1 2009 2009
dbSNP: rs11075985
rs11075985
FTO
3 1.000 0.080 16 53771295 intron variant C/A snv 0.42 0.700 1.000 1 2009 2009
dbSNP: rs11075987
rs11075987
FTO
2 1.000 0.080 16 53781249 intron variant T/A;G snv 0.59 0.700 1.000 1 2009 2009
dbSNP: rs11075989
rs11075989
FTO
3 0.925 0.120 16 53785965 intron variant C/A;T snv 0.700 1.000 1 2009 2009
dbSNP: rs11075990
rs11075990
FTO
6 0.925 0.120 16 53785981 intron variant A/G snv 0.41 0.700 1.000 1 2009 2009
dbSNP: rs1121980
rs1121980
FTO
18 0.807 0.240 16 53775335 intron variant G/A;C snv 0.700 1.000 1 2009 2009
dbSNP: rs11642841
rs11642841
FTO
3 0.925 0.120 16 53811575 intron variant C/A;G snv 0.700 1.000 1 2009 2009
dbSNP: rs12149832
rs12149832
FTO
8 0.851 0.120 16 53808996 intron variant G/A snv 0.31 0.700 1.000 1 2009 2009
dbSNP: rs12446228
rs12446228
FTO
2 1.000 0.080 16 53766475 intron variant A/G;T snv 0.700 1.000 1 2009 2009
dbSNP: rs12954782
rs12954782 		2 1.000 0.080 18 60196859 non coding transcript exon variant C/G snv 0.22 0.700 1.000 1 2009 2009
dbSNP: rs12969709
rs12969709 		4 1.000 0.080 18 60192330 upstream gene variant C/A snv 0.21 0.700 1.000 1 2009 2009
dbSNP: rs1457489
rs1457489 		3 1.000 0.080 18 60194728 upstream gene variant G/A snv 0.29 0.700 1.000 1 2009 2009