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: rs9930506
rs9930506
FTO
16 0.776 0.360 16 53796553 intron variant A/G snv 0.36 0.700 1.000 1 2007 2007
dbSNP: rs12110693
rs12110693
LOC105377979
2 6 121837124 intergenic variant G/A snv 0.23 0.700 1.000 1 2009 2009
dbSNP: rs12731740
rs12731740
MIR29B2CHG
2 1 207851475 intron variant C/T snv 9.1E-02 0.700 1.000 1 2009 2009
dbSNP: rs17249754
rs17249754
ATP2B1
12 0.882 0.120 12 89666809 intron variant G/A snv 0.15 0.700 1.000 1 2009 2009
dbSNP: rs2074356
rs2074356
HECTD4
18 0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03 0.800 1.000 1 2009 2009
dbSNP: rs7776725
rs7776725
FAM3C
4 1.000 0.080 7 121393067 intron variant T/C snv 0.28 0.700 1.000 1 2009 2009
dbSNP: rs9939609
rs9939609
FTO
98 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.700 1.000 1 2009 2009
dbSNP: rs1034207
rs1034207 		1 6 127016554 intron variant C/A;G;T snv 0.94 0.700 1.000 1 2010 2010
dbSNP: rs11154370
rs11154370 		1 6 126846446 intron variant A/G;T snv 0.700 1.000 1 2010 2010
dbSNP: rs2076529
rs2076529
BTNL2 ; TSBP1-AS1
2 1.000 0.120 6 32396178 synonymous variant T/C snv 0.41 0.39 0.800 1.000 1 2010 2010
dbSNP: rs4580892
rs4580892 		3 6 127088737 intron variant C/T snv 0.32 0.700 1.000 1 2010 2010
dbSNP: rs4846567
rs4846567 		1 1 219577375 regulatory region variant G/T snv 0.23 0.800 1.000 1 2010 2010
dbSNP: rs6701231
rs6701231
TBX15
1 1 118953038 intron variant C/A;G snv 0.700 1.000 1 2010 2010
dbSNP: rs6784615
rs6784615
NISCH
2 1.000 0.080 3 52472410 intron variant C/T snv 0.96 0.96 0.800 1.000 1 2010 2010
dbSNP: rs6795735
rs6795735
ADAMTS9-AS2
7 0.882 0.120 3 64719689 intron variant C/A;G;T snv 0.800 1.000 1 2010 2010
dbSNP: rs987763
rs987763
LOC105377989
1 6 126960402 intron variant C/A;T snv 0.700 1.000 1 2010 2010
dbSNP: rs10894604
rs10894604
OPCML
1 11 132771851 non coding transcript exon variant T/G snv 0.26 0.800 1.000 1 2013 2013
dbSNP: rs11016883
rs11016883
MGMT
1 10 129702676 intron variant G/C snv 0.38 0.700 1.000 1 2013 2013
dbSNP: rs17213965
rs17213965
MYH11
1 16 15788110 intron variant C/T snv 0.24 0.800 1.000 1 2013 2013
dbSNP: rs2820443
rs2820443 		8 0.882 0.120 1 219580167 regulatory region variant T/C snv 0.23 0.700 1.000 1 2013 2013
dbSNP: rs2820464
rs2820464
LYPLAL1-AS1
1 1 219519878 intergenic variant G/A;C snv 0.800 1.000 1 2013 2013
dbSNP: rs5980075
rs5980075 		1 X 14932409 intergenic variant A/G snv 0.700 1.000 1 2013 2013
dbSNP: rs6717858
rs6717858
COBLL1
1 2 164683151 3 prime UTR variant T/A;C snv 0.700 1.000 1 2013 2013
dbSNP: rs6931262
rs6931262
RREB1
1 6 7217284 non coding transcript exon variant C/T snv 0.10 0.800 1.000 1 2013 2013
dbSNP: rs765684
rs765684
LOC105374811
1 2 75232542 intergenic variant A/C;G snv 0.700 1.000 1 2013 2013