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: rs2245667
rs2245667
PDGFRL
1 8 17603819 intron variant C/G snv 0.64 0.700 1.000 1 2009 2009
dbSNP: rs2605100
rs2605100
LYPLAL1-AS1 ; LOC107985272
3 1.000 0.080 1 219470882 intergenic variant A/G snv 0.77 0.700 1.000 1 2009 2009
dbSNP: rs2943650
rs2943650 		6 0.827 0.120 2 226241205 intergenic variant C/T snv 0.58 0.700 1.000 1 2011 2011
dbSNP: rs4754373
rs4754373 		1 11 109022119 intron variant C/T snv 0.21 0.700 1.000 1 2009 2009
dbSNP: rs534870
rs534870 		2 1.000 0.080 13 80385072 intergenic variant G/A snv 0.71 0.700 1.000 1 2011 2011
dbSNP: rs545854
rs545854 		4 0.882 0.160 8 10002570 intron variant G/C snv 0.85 0.700 1.000 1 2009 2009
dbSNP: rs6429082
rs6429082
TBCE
2 1.000 0.080 1 235436814 intron variant T/C snv 0.55 0.700 1.000 1 2009 2009
dbSNP: rs7970350
rs7970350
HMGA2
5 12 65966384 downstream gene variant C/T snv 0.48 0.700 1.000 1 2009 2009
dbSNP: rs8050136
rs8050136
FTO
32 0.716 0.560 16 53782363 intron variant C/A snv 0.40 0.700 1.000 1 2011 2011
dbSNP: rs987237
rs987237
TFAP2B
10 0.925 0.120 6 50835337 intron variant A/G snv 0.17 0.700 1.000 1 2009 2009