Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3818416
EDNRB-AS1 ; EDNRB
1.000 0.080 13 77900333 intron variant A/C snv 0.75 3
rs6544334
SLC8A1
2 40369384 intron variant A/C snv 0.68 1
rs622871
CYP21A2 ; C2
1.000 0.040 6 31910718 intron variant A/C;G snv 2
rs6946091 7 150987258 upstream gene variant A/C;G snv 1
rs16892496
TRHR
1.000 0.080 8 109097622 intron variant A/C;G;T snv 2
rs9512696
MTIF3
13 27438390 intron variant A/C;G;T snv 1
rs2005172
GH1
17 63918895 intron variant A/C;T snv 1
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 19
rs543874 1.000 0.080 1 177920345 upstream gene variant A/G snv 0.21 11
rs724016
ZBTB38
1.000 0.040 3 141386728 5 prime UTR variant A/G snv 0.52 5
rs12889267
ARHGEF40
14 21074607 missense variant A/G snv 0.16 0.13 4
rs2207139 1.000 0.080 6 50877777 intergenic variant A/G snv 0.16 4
rs13245690
CPED1
7 121145010 intron variant A/G snv 0.32 3
rs115179432
LTBP1
2 33123612 intron variant A/G snv 5.6E-02 2
rs12879423 14 25458626 intergenic variant A/G snv 0.55 2
rs2943656 1.000 0.080 2 226257202 regulatory region variant A/G snv 0.63 2
rs3765350
WNT4
1 22120823 intron variant A/G snv 0.22 2
rs55745410
PHC2
1 33337216 intron variant A/G snv 0.28 2
rs62372052 5 42724192 upstream gene variant A/G snv 6.9E-02 2
rs10068807 5 55581157 intergenic variant A/G snv 0.70 1
rs1108548
LINC02869
1 218461445 intron variant A/G snv 0.40 1
rs11597119
SLF2
10 100914591 intron variant A/G snv 0.35 1
rs263137
LOC153910
6 142632820 intron variant A/G snv 0.42 1
rs61838774
LYPLAL1 ; LYPLAL1-AS1
1 219440433 intron variant A/G snv 0.27 1
rs66827053
LOC105371795
17 45173286 upstream gene variant A/G snv 0.20 1