Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17030613
CAPZA1
1 112648185 intron variant A/C snv 0.19 7
rs17249754
ATP2B1
0.882 0.120 12 89666809 intron variant G/A snv 0.15 7
rs17367504
MTHFR
1.000 0.040 1 11802721 intron variant A/G snv 0.14 7
rs2383207
CDKN2B-AS1
0.695 0.280 9 22115960 intron variant A/G snv 0.64 7
rs6015450
ZNF831
20 59176062 intron variant A/G snv 0.14 7
rs805303
BAG6
0.925 0.160 6 31648589 intron variant G/A snv 0.45 7
rs11613352
R3HDM2
0.827 0.160 12 57398797 intron variant C/T snv 0.19 6
rs12413409
CNNM2
0.790 0.200 10 102959339 intron variant G/A snv 9.0E-02 6
rs1327235 20 10988382 intron variant A/G snv 0.46 6
rs17514846
FURIN
0.882 0.120 15 90873320 intron variant C/A;G snv 6
rs1800588
ALDH1A2 ; LIPC
0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 6
rs1887320 20 10985350 intron variant G/A snv 0.46 6
rs26528
IL27
0.807 0.200 16 28506388 intron variant T/C snv 0.43 6
rs4409766
BORCS7-ASMT ; BORCS7
1.000 0.040 10 102856906 intron variant T/C snv 0.14 6
rs7647305
DGKG
1.000 0.080 3 186116501 intron variant T/C snv 0.74 6
rs932764
PLCE1
10 94136183 intron variant A/G snv 0.38 6
rs10184428 2 164155317 intron variant C/A;G snv 5
rs16849225 2 164050310 intron variant C/T snv 0.19 5
rs1731249
KCNK3
2 26697157 intron variant T/A snv 0.48 5
rs2131925
DOCK7
1 62560271 intron variant G/T snv 0.57 5
rs2237892
KCNQ1
0.790 0.320 11 2818521 intron variant C/T snv 9.2E-02 5
rs3790604
WNT2B
1 112504257 intron variant C/A snv 7.8E-02 5
rs6021247
NFATC2
1.000 0.080 20 51492442 intron variant G/A snv 0.65 5
rs661348
LSP1
11 1884062 intron variant T/C snv 0.43 0.37 5
rs6742078
UGT1A3 ; UGT1A7 ; UGT1A8 ; UGT1A10 ; UGT1A6 ; UGT1A4 ; UGT1A9 ; UGT1A1 ; UGT1A5
0.807 0.240 2 233763993 intron variant G/T snv 0.36 5