Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 3
rs10745332
CAPZA1
1 112646431 intron variant G/A snv 0.77 3
rs10757274
CDKN2B-AS1
0.701 0.320 9 22096056 intron variant A/G snv 0.41 3
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40 4
rs10770141
MIR4686 ; TH
1.000 0.120 11 2172610 upstream gene variant A/C;G snv 1
rs10776752
WNT2B
1 112501706 intron variant G/T snv 8.8E-02 4
rs10785581
LOC105369743
12 45537190 intron variant C/A;G snv 1
rs10857147 1.000 0.040 4 80259918 intergenic variant A/T snv 0.25 9
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 11
rs10948071
ZNF318
6 43312975 intron variant C/T snv 0.46 4
rs11014166
CACNB2
0.882 0.040 10 18419869 intron variant A/T snv 0.27 8
rs11020821 11 94538497 intergenic variant C/A snv 0.28 1
rs11066280
HECTD4
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 18
rs11067763
LOC105370003
12 115760536 intron variant A/G snv 0.16 3
rs11099098 0.925 0.120 4 80248758 intergenic variant G/C;T snv 8
rs11105364
ATP2B1
12 89675499 intron variant T/G snv 0.15 4
rs11105368
ATP2B1
12 89680664 intron variant G/A;C snv 1
rs11124945
PLEKHH2
1.000 0.040 2 43650017 intron variant A/G snv 0.21 3
rs11191514
CNNM2
10 103013607 intron variant C/G;T snv 1
rs11191548
CNNM2
0.882 0.080 10 103086421 3 prime UTR variant T/C snv 8.6E-02 7
rs11191580
NT5C2
0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02 12
rs11191593
NT5C2
10 103179458 intron variant T/C snv 9.0E-02 4
rs11203368
PADI4
0.925 0.200 1 17340013 intron variant C/T snv 0.57 1
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 8
rs1122608
SMARCA4
0.763 0.120 19 11052925 intron variant G/T snv 0.18 8