Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10974438
GLIS3
0.925 0.120 9 4291928 intron variant A/C snv 0.29 3
rs11591710 0.882 0.160 10 103927874 intergenic variant A/C snv 0.16 3
rs1372503923
ITGA2
0.925 0.160 5 53048731 missense variant A/C snv 3
rs16860234
IGF2BP2
0.925 0.080 3 185793096 intron variant A/C snv 0.33 3
rs2275703
CASQ1
0.925 0.080 1 160195305 intron variant A/C snv 0.38 3
rs9896052 0.882 0.160 17 75422781 intergenic variant A/C snv 0.50 3
rs10517030
PPARGC1A
0.925 0.120 4 23961283 intergenic variant A/C snv 6.9E-02 2
rs115689251
LOC107985068
1.000 0.080 17 36032377 intergenic variant A/C snv 1.0E-02 2
rs118204073
LPL
0.925 0.120 8 19951825 missense variant A/C snv 4.0E-06 7.0E-06 2
rs11873305 1.000 0.080 18 60381959 intron variant A/C snv 0.12 2
rs151290
KCNQ1
1.000 0.080 11 2800385 intron variant A/C snv 0.67 2
rs1541276
MC5R
0.925 0.120 18 13825728 splice region variant A/C snv 0.17 0.19 2
rs75298135 1.000 0.080 5 28184372 intergenic variant A/C snv 1.3E-02 2
rs7929543 0.925 0.120 11 49329474 intron variant A/C snv 0.12 2
rs9472719 1.000 0.080 6 46183649 regulatory region variant A/C snv 0.32 2
rs9942471 0.925 0.160 6 89238513 intergenic variant A/C snv 0.37 2
rs10100265
PINX1
1.000 0.080 8 10775649 intron variant A/C snv 0.60 1
rs1071592
AHSG
1.000 0.080 3 186620636 synonymous variant A/C snv 0.76 0.77 1
rs13083654
UBE2E2
1.000 0.080 3 23245193 intron variant A/C snv 0.11 1
rs141205818
ADIPOQ ; ADIPOQ-AS1
1.000 0.080 3 186854691 missense variant A/C snv 3.9E-04 1.8E-04 1
rs1424642 1.000 0.080 2 57069423 intergenic variant A/C snv 0.78 1
rs16856187 1.000 0.080 2 168913876 upstream gene variant A/C snv 6.0E-02 1
rs202178099 1.000 0.080 5 50927276 downstream gene variant A/C snv 3.2E-02 1
rs2283228
KCNQ1
1.000 0.080 11 2828300 intron variant A/C snv 0.10 1
rs2779772
CNTLN
1.000 0.080 9 17147193 intron variant A/C snv 0.21 1