Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 73
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 30
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 27
rs28929474
SERPINA1
0.708 0.320 14 94378610 missense variant C/G;T snv 2.8E-05; 1.1E-02 23
rs79105258
CUX2
12 111280427 intron variant C/A;T snv 23
rs1728918 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 19
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 19
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 19
rs478442 0.851 0.120 2 21176344 intergenic variant G/C;T snv 18
rs765547 0.827 0.160 8 20008763 intergenic variant G/A;C;T snv 18
rs13114738
SLC39A8
0.851 0.120 4 102363708 intron variant C/A;T snv 16
rs4704221
CERT1
0.851 0.120 5 75463358 intron variant T/A;C snv 16
rs4905014
ITPK1
0.851 0.120 14 92945686 intron variant G/A;C snv 16
rs7115242
SIK3
0.851 0.120 11 117037567 intron variant A/G;T snv 16
rs198851
H4C3
6 26104404 downstream gene variant T/A;C;G snv 15
rs11556924
ZC3HC1
0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 14
rs7137828
ATXN2
0.763 0.200 12 111494996 intron variant C/A;T snv 14
rs1378942
CSK
0.790 0.240 15 74785026 intron variant C/A;T snv 10
rs185819
TNXB
0.851 0.200 6 32082290 missense variant T/A;C;G snv 8.2E-06; 0.58; 4.1E-06 10
rs2521501
FES
0.925 0.080 15 90894158 intron variant A/C;T snv 10
rs2571445
TNS1
0.925 0.080 2 217818431 missense variant A/G;T snv 0.62 10
rs2681492
ATP2B1
0.925 0.040 12 89619312 intron variant T/C;G snv 10
rs633185
ARHGAP42
0.925 0.080 11 100722807 intron variant G/A;C snv 10
rs16998073 0.925 0.120 4 80263187 upstream gene variant A/G;T snv 9
rs11099098 0.925 0.120 4 80248758 intergenic variant G/C;T snv 8