Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs312262690
ANTXR2
0.752 0.320 4 79984831 frameshift variant -/G;GG delins 1.7E-05 28
rs17030613
CAPZA1
1 112648185 intron variant A/C snv 0.19 7
rs4833103
TLR1
0.925 0.160 4 38813881 intron variant A/C snv 0.64 4
rs8098380
YES1
18 721563 downstream gene variant A/C snv 0.33 4
rs113296370
PLEKHH2
1.000 0.040 2 43636315 upstream gene variant A/C snv 0.17 3
rs12500426
PDLIM5
0.851 0.240 4 94593458 intron variant A/C snv 0.54 3
rs4387287
STN1
10 103918139 5 prime UTR variant A/C snv 0.69 3
rs4686340
SRGAP3
3 9303534 intron variant A/C snv 0.80 2
rs121912594
CPS1
0.882 0.160 2 210675762 missense variant A/C snv 1
rs403814
L3MBTL4
18 6282594 intron variant A/C snv 0.27 1
rs729302 0.827 0.160 7 128928906 intergenic variant A/C snv 0.28 1
rs2932538
MOV10
1 112673921 intron variant A/C;G snv 4
rs6418
GML ; CYP11B2
8 142914947 intron variant A/C;G snv 0.42 4
rs7006531 8 94098516 intron variant A/C;G snv 3
rs2069837
IL6-AS1 ; IL6
0.724 0.520 7 22728408 intron variant A/C;G snv 2
rs10770141
MIR4686 ; TH
1.000 0.120 11 2172610 upstream gene variant A/C;G snv 1
rs1859168
HOTTIP
0.790 0.160 7 27202740 non coding transcript exon variant A/C;G;T snv 4
rs7310409
HNF1A
0.925 0.160 12 120987058 intron variant A/C;G;T snv 4
rs17465637
MIA3
0.790 0.200 1 222650187 intron variant A/C;G;T snv 0.64; 6.4E-06 3
rs12715461
CACNA1D
3 53544856 intron variant A/C;G;T snv 1
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 1
rs2521501
FES
0.925 0.080 15 90894158 intron variant A/C;T snv 10
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 3
rs12579302
ATP2B1
0.851 0.120 12 89656726 intron variant A/G snv 0.15 19
rs28933386
PTPN11
0.752 0.400 12 112477719 missense variant A/G snv 1.2E-05 7.0E-06 14