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: rs10447248
rs10447248 		1 5 108580035 intergenic variant A/G snv 0.70 0.800 1.000 1 2011 2011
dbSNP: rs10794657
rs10794657 		1 1 24299684 intergenic variant A/G snv 0.75 0.800 1.000 1 2012 2012
dbSNP: rs10937273
rs10937273 		4 0.882 0.160 3 186831906 downstream gene variant G/A snv 0.33 0.800 1.000 1 2014 2014
dbSNP: rs1108842
rs1108842
GNL3 ; PBRM1
2 3 52686064 5 prime UTR variant A/C;G;T snv 0.49; 4.0E-06 0.800 1.000 1 2012 2012
dbSNP: rs11168618
rs11168618 		1 12 48539450 intergenic variant C/T snv 0.33 0.800 1.000 1 2014 2014
dbSNP: rs1187415
rs1187415
RFLNA ; ZNF664 ; ZNF664-RFLNA
1 12 124006982 intron variant G/C snv 0.60 0.800 1.000 1 2014 2014
dbSNP: rs11924390
rs11924390
LOC105374258
1 3 186715310 intron variant T/A;C snv 0.800 1.000 1 2010 2010
dbSNP: rs1515110
rs1515110 		1 2 226257500 intergenic variant G/A;C;T snv 0.800 1.000 1 2012 2012
dbSNP: rs1648707
rs1648707 		3 0.925 0.080 3 186833922 intergenic variant A/C snv 0.43 0.800 1.000 1 2009 2009
dbSNP: rs182052
rs182052
ADIPOQ
19 0.701 0.440 3 186842993 intron variant G/A snv 0.38 0.800 1.000 1 2012 2012
dbSNP: rs2468677
rs2468677 		1 8 139507274 downstream gene variant G/T snv 0.54 0.800 1.000 1 2011 2011
dbSNP: rs2590838
rs2590838
PBRM1
3 3 52588070 intron variant G/A snv 0.55 0.800 1.000 1 2012 2012
dbSNP: rs266717
rs266717
LINC02043
1 3 186812695 intron variant T/C;G snv 0.57 0.800 1.000 1 2009 2009
dbSNP: rs266719
rs266719
EIF4A2 ; SNORD2
1 3 186783859 non coding transcript exon variant T/C snv 0.84 0.800 1.000 1 2014 2014
dbSNP: rs2791553
rs2791553
LYPLAL1-AS1 ; LOC107985272
1 1 219502700 intergenic variant A/G snv 0.57 0.800 1.000 1 2012 2012
dbSNP: rs2980879
rs2980879 		3 0.925 0.120 8 125469233 intron variant A/T snv 0.69 0.800 1.000 1 2012 2012
dbSNP: rs3001032
rs3001032
LYPLAL1-AS1
1 1 219554437 upstream gene variant T/C snv 0.35 0.800 1.000 1 2012 2012
dbSNP: rs3943077
rs3943077
LINC01153
1 10 121185572 non coding transcript exon variant A/G snv 0.59 0.800 1.000 1 2014 2014
dbSNP: rs4301033
rs4301033
LINC01214 ; LOC107986141
1 3 150324831 regulatory region variant G/A snv 0.12 0.800 1.000 1 2012 2012
dbSNP: rs4311394
rs4311394
ARL15
2 1.000 0.080 5 54004832 intron variant A/G snv 0.27 0.800 1.000 1 2009 2009
dbSNP: rs4805885
rs4805885
PEPD
1 19 33415217 intron variant T/C snv 0.59 0.800 1.000 1 2012 2012
dbSNP: rs592423
rs592423 		6 6 139519556 intron variant A/C snv 0.50 0.800 1.000 1 2012 2012
dbSNP: rs6450176
rs6450176
ARL15
4 5 54002195 intron variant G/A snv 0.27 0.800 1.000 1 2012 2012
dbSNP: rs6488898
rs6488898
ATP6V0A2 ; LOC105370042
1 12 123719285 intron variant G/A snv 0.95 0.800 1.000 1 2012 2012
dbSNP: rs6773957
rs6773957
ADIPOQ ; ADIPOQ-AS1
2 1.000 0.040 3 186855916 3 prime UTR variant A/C;G snv 0.55 0.800 1.000 1 2009 2009