Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10508503 1.000 0.080 10 16257952 intergenic variant C/A;T snv 1
rs11084753 1.000 0.080 19 33831232 intergenic variant A/C;G;T snv 0.65 1
rs12461383 19 40864433 intron variant C/G snv 0.42 1
rs1394371 0.925 0.080 15 78432127 intergenic variant C/T snv 0.22 1
rs1451240 0.925 0.080 8 42691568 intergenic variant A/G snv 0.64 1
rs1678618 10 72046530 intergenic variant A/G snv 0.39 1
rs17700144 1.000 0.080 18 60144750 intron variant G/A snv 0.14 1
rs2869032 15 78422219 regulatory region variant C/G;T snv 1
rs3025343 9 133613233 non coding transcript exon variant G/A snv 7.0E-02 1
rs4105144 0.827 0.160 19 40852719 intron variant T/C snv 1
rs4887053 0.925 0.080 15 78420357 regulatory region variant A/C;T snv 1
rs5019044 15 78503940 upstream gene variant T/A snv 0.21 1
rs547843 15 26178900 regulatory region variant C/G;T snv 1
rs6474412 0.925 0.120 8 42695355 upstream gene variant C/T snv 0.64 1
rs6548238 0.882 0.200 2 634905 TF binding site variant T/C snv 0.85 1
rs8102683 19 40857860 intron variant T/C snv 0.75 1
rs848353 1.000 0.080 7 108908603 upstream gene variant A/G snv 0.14 1
rs12903203
ADAMTS7
15 78792591 intron variant T/C snv 0.31 1
rs1994016
ADAMTS7
0.851 0.160 15 78787892 intron variant C/T snv 0.30 1
rs2277545
ADAMTS7
15 78791249 intron variant T/C snv 0.33 0.31 1
rs7177699
ADAMTS7
15 78797392 intron variant T/C snv 0.33 1
rs9931989
ATP2A1
16 28894763 intron variant G/C snv 0.68 1
rs6437740
BBX
3 107746970 intron variant T/C snv 0.25 1
rs3101457
C1orf100
1 244369912 intron variant G/A snv 0.80 1
rs4712652
CASC15
1.000 0.080 6 22078386 intron variant G/A snv 0.64 1