Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1905786
TNFRSF11B
1.000 0.040 8 118939453 intron variant T/A;C snv 2
rs1913707 0.925 0.040 4 13037816 intergenic variant A/G snv 0.40 2
rs2276454
COL2A1 ; LOC105369752
0.925 0.040 12 47982508 synonymous variant G/A snv 0.39 0.38 2
rs2785988 0.925 0.040 1 219570796 intergenic variant C/A snv 0.23 2
rs2830585
ADAMTS5
1.000 0.040 21 26932893 missense variant C/T snv 0.12 0.12 2
rs3771501
TGFA
0.925 0.040 2 70490521 intron variant A/G snv 0.60 2
rs4072286 1.000 0.040 8 141726333 regulatory region variant G/A;T snv 2
rs4144782
EN1
0.925 0.040 2 118844296 non coding transcript exon variant A/C;G snv 2
rs4233367
ADAMTS4
0.925 0.040 1 161193247 missense variant T/A;C snv 0.67 2
rs4238326
ALDH1A2
0.925 0.040 15 58043802 intron variant T/C snv 0.28 2
rs4721
LRRC61 ; RARRES2
1.000 0.040 7 150338437 missense variant T/A;C;G snv 0.42 0.47 2
rs4747096
ADAMTS14
0.925 0.040 10 70758253 missense variant A/G;T snv 0.19 0.19 2
rs4907986
COL11A1
0.925 0.040 1 103084077 intron variant C/T snv 0.49 2
rs6773957
ADIPOQ ; ADIPOQ-AS1
1.000 0.040 3 186855916 3 prime UTR variant A/C;G snv 0.55 2
rs7164503
ANP32A
0.925 0.040 15 68789051 intron variant T/C snv 0.27 2
rs835487
CHST11
0.925 0.040 12 104666989 intron variant A/G snv 0.43 2
rs912428
LRCH1
0.925 0.040 13 46593768 intron variant A/G snv 0.84 2
rs919642
LOC105376225
1.000 0.040 9 114148867 intergenic variant A/T snv 0.22 2
rs9350591 0.925 0.040 6 75531811 intergenic variant C/A;T snv 0.12 2
rs10172410
ITGA4
1.000 0.040 2 181487841 intron variant T/C snv 0.45 1
rs10218792
KIF26B
1.000 0.040 1 245587630 intron variant T/G snv 0.26 1
rs1032128
TNFRSF11B
1.000 0.040 8 118939534 intron variant G/A snv 0.30 1
rs1034762
COL2A1
1.000 0.040 12 47995860 intron variant A/C snv 0.74 0.79 1
rs10401670
MCEMP1
1.000 0.040 19 7677916 intron variant T/C;G snv 0.49 1
rs10502437
TMEM241
1.000 0.040 18 23390742 intron variant G/A snv 0.30 1