Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10122541 1.000 0.080 9 97865986 intergenic variant G/A snv 0.68 1
rs73227498
EPB41L4A
1.000 0.080 5 112150207 intron variant A/T snv 0.11 1
rs1443435
FOXE1
1.000 0.080 9 97855301 3 prime UTR variant T/C snv 0.63 1
rs2466076
NRG1
1.000 0.080 8 32575278 intron variant G/T snv 0.53 1
rs12129938
PCNX2
1.000 0.080 1 233276815 intron variant A/G snv 0.20 1
rs2289261
SMAD3
1.000 0.080 15 67165147 intron variant G/C;T snv 0.61 1
rs10984103 0.925 0.080 9 97876993 TF binding site variant A/C snv 0.68 2
rs7866436 0.925 0.080 9 97887814 intergenic variant G/A snv 0.70 2
rs7902587 0.925 0.080 10 103934543 intergenic variant C/T snv 0.11 2
rs925487 0.925 0.080 9 97874116 regulatory region variant C/A;T snv 2
rs11693806
DIRC3
0.925 0.120 2 217427435 non coding transcript exon variant C/A;G snv 0.65 2
rs6759952
DIRC3
1.000 0.080 2 217406996 intron variant T/A;C snv 2
rs1179469165
LOC101928462 ; TSHR
0.925 0.080 14 81143917 missense variant C/T snv 8.0E-06 7.0E-06 2
rs368187
LOC105370452
0.925 0.080 14 36063370 non coding transcript exon variant G/A;C;T snv 2
rs10983700
PTCSC2
1.000 0.080 9 97775173 intron variant T/A;C snv 2
rs12348691
PTCSC2
0.925 0.120 9 97846400 intron variant G/A snv 0.63 2
rs1588635
PTCSC2
1.000 0.080 9 97775520 intron variant A/C snv 0.72 2
rs7024345
PTCSC2
0.925 0.080 9 97832956 intron variant A/G snv 0.82 2
rs7030280
PTCSC2
1.000 0.080 9 97772985 intron variant C/T snv 0.72 2
rs7848973
PTCSC2
0.925 0.080 9 97826557 intron variant A/G snv 0.67 2
rs2145418 0.882 0.080 1 118422631 intergenic variant C/A snv 0.78 3
rs747463591
CCDC6
0.882 0.080 10 59906391 missense variant C/A;G;T snv 4.9E-06; 9.9E-06 3
rs78929565
CLOCK
0.882 0.080 4 55539035 intron variant C/A;T snv 3
rs1032006770
EGFR
0.882 0.080 7 55160171 missense variant A/G snv 4.0E-06 7.0E-06 3
rs1031583860
GLYAT
0.882 0.080 11 58709815 missense variant T/C snv 3