Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2124459
CBS
0.827 0.200 21 43055604 3 prime UTR variant T/C snv 0.36 5
rs2326398
CRISPLD2
0.827 0.200 16 84869111 intron variant A/G snv 0.37 5
rs493760
DROSHA
0.851 0.200 5 31436933 intron variant C/T snv 0.74 5
rs2013162
IRF6
0.827 0.280 1 209795339 synonymous variant C/A;T snv 0.41; 1.6E-05 5
rs13041247
LOC102724968
0.851 0.200 20 40640434 regulatory region variant T/C snv 0.36 5
rs2269529
MYH9 ; MIR6819
0.851 0.200 22 36288308 missense variant T/C snv 0.26 0.18 5
rs1474322770
NKX2-1 ; NKX2-1-AS1 ; SFTA3
0.827 0.240 14 36519251 missense variant G/A snv 5
rs2239907
SARM1 ; SLC46A1
0.851 0.200 17 28398728 3 prime UTR variant T/C snv 0.53 5
rs739439
SLC46A1 ; SARM1
0.851 0.200 17 28396803 3 prime UTR variant C/T snv 0.13 5
rs11466285
TGFA
0.851 0.200 2 70450307 3 prime UTR variant A/C;G snv 5
rs2166975
TGFA
0.827 0.240 2 70450862 synonymous variant G/A snv 0.24 0.23 5
rs3771523
TGFA
0.851 0.200 2 70450336 3 prime UTR variant C/T snv 0.14 5
rs12543318 0.882 0.120 8 87856112 intergenic variant C/A snv 0.68 4
rs227731 0.882 0.120 17 56695877 intergenic variant T/A;G snv 4
rs8049367 0.851 0.240 16 3930444 downstream gene variant T/C snv 0.37 4
rs28937575
FOXE1 ; PTCSC2
0.851 0.280 9 97854084 missense variant G/A snv 4
rs6072081
LOC102724968
0.851 0.120 20 40632414 intergenic variant A/G snv 0.49 4
rs197204
MCUB
0.851 0.200 4 109576918 intron variant C/G snv 0.52 4
rs4791774
NTN1
0.882 0.240 17 9028802 intron variant A/C;G snv 4
rs10512248
PTCH1
0.925 0.120 9 95497421 intron variant T/A;G snv 4
rs705704
RPS26 ; LOC105369780
0.882 0.240 12 56041628 non coding transcript exon variant G/A snv 0.26 4
rs7078160
SHTN1
0.851 0.120 10 117068049 intron variant G/A snv 0.19 4
rs8179096
TIMP2
0.851 0.200 17 78925567 upstream gene variant G/A;C snv 4
rs1139
ZNF385B
0.851 0.200 2 179745354 intron variant C/T snv 0.22 4
rs6757845
ZNF385B
0.851 0.200 2 179449268 intron variant T/C snv 0.66 4