Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17482753 1.000 0.080 8 19975135 regulatory region variant G/T snv 8.8E-02 8
rs649129 1.000 0.080 9 133278860 upstream gene variant T/C;G snv 8
rs11558471
LOC105375716 ; SLC30A8
1.000 0.080 8 117173494 3 prime UTR variant A/G snv 0.25 5
rs13389219
COBLL1
1.000 0.080 2 164672366 intron variant C/T snv 0.47 5
rs3794991
GATAD2A
1.000 0.080 19 19499787 intron variant C/G;T snv 7.4E-02 5
rs9368222
CDKAL1
1.000 0.080 6 20686765 intron variant C/A;T snv 5
rs10224002
PRKAG2
0.925 0.080 7 151717955 intron variant A/G snv 0.31 4
rs11603334
ARAP1
1.000 0.080 11 72721940 5 prime UTR variant G/A snv 0.12 4
rs11708067
ADCY5
0.882 0.080 3 123346931 intron variant A/G snv 0.19 4
rs1799884
GCK
1.000 0.080 7 44189469 intron variant C/T snv 0.17 4
rs2000999
HPR ; TXNL4B
1.000 0.080 16 72074194 intron variant G/A snv 0.16 4
rs2191349 1.000 0.080 7 15024684 intergenic variant G/T snv 0.54 4
rs340874
PROX1 ; PROX1-AS1
0.882 0.080 1 213985913 non coding transcript exon variant T/C snv 0.40 4
rs10195252
COBLL1
0.925 0.080 2 164656581 intron variant T/C snv 0.48 3
rs10244051 1.000 0.080 7 15024208 intergenic variant T/A;G snv 3
rs10885122 1.000 0.080 10 111282335 intergenic variant T/G snv 0.71 3
rs11257655 1.000 0.080 10 12265895 TF binding site variant C/T snv 0.23 3
rs11605924
CRY2
1.000 0.080 11 45851540 intron variant A/C snv 0.39 3
rs11717195
ADCY5
1.000 0.080 3 123363551 intron variant T/C snv 0.19 3
rs1552224
ARAP1
1.000 0.080 11 72722053 5 prime UTR variant A/C snv 0.12 3
rs17168486
DGKB
1.000 0.080 7 14858657 intron variant C/T snv 0.18 3
rs17238484
HMGCR
1.000 0.080 5 75352671 intron variant G/T snv 0.22 3
rs174455
FADS3
1.000 0.080 11 61888645 intron variant G/A;C snv 3
rs1783598
FCHSD2
1.000 0.080 11 73140418 intron variant C/G;T snv 3
rs2304130
ZNF101
1.000 0.080 19 19678719 splice region variant A/G snv 0.10 0.12 3