Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs756421370
MECR
0.807 0.120 1 29200513 splice donor variant -/A delins 1.4E-04 6.3E-05 8
rs1554208945
ZNF292
0.752 0.240 6 87260207 missense variant A/C snv 26
rs6568431
ATG5
0.790 0.320 6 106140931 intron variant A/C snv 0.61 3
rs121918455
PTPN11
0.695 0.440 12 112477720 missense variant A/C;G snv 31
rs2069837
IL6-AS1 ; IL6
0.724 0.520 7 22728408 intron variant A/C;G snv 2
rs3024490
IL10 ; IL19
0.742 0.520 1 206771966 intron variant A/C;G;T snv 1
rs1131692230
PDHA1
0.807 0.160 X 19353124 missense variant A/G snv 9
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 2
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 1
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 6
rs767399782
TUBB4A
0.925 0.120 19 6495736 missense variant C/A;T snv 4.0E-06 2
rs765462548
STN1
0.882 0.160 10 103898989 missense variant C/A;T snv 4.0E-06; 2.4E-05 1
rs1057519583
STN1
0.882 0.160 10 103900115 missense variant C/G snv 1
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 1
rs780533096
MIPEP
0.701 0.600 13 23886338 missense variant C/G;T snv 4.8E-06; 9.6E-06 44
rs80338700
PMM2
0.851 0.200 16 8806398 missense variant C/G;T snv 4.0E-06; 2.4E-05 7
rs1476413
MTHFR
0.790 0.360 1 11792243 intron variant C/G;T snv 4.0E-06; 0.26 0.23 1
rs606231435
ATP1A3
0.827 0.240 19 41970539 missense variant C/T snv 17
rs1553630279
CTNNB1
0.807 0.160 3 41225049 stop gained C/T snv 7
rs1555303073
COL4A1
0.851 0.120 13 110176912 missense variant C/T snv 6
rs1799724
LTA ; TNF
0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 2
rs2853749
SPP1
0.882 0.160 4 87976662 intron variant C/T snv 0.34 2
rs10431386
MLEC
1.000 0.040 12 120691123 intron variant C/T snv 0.34 1
rs121918399
APOE
0.925 0.120 19 44907843 missense variant C/T snv 8.0E-06 1
rs28934906
MECP2
0.716 0.320 X 154031355 missense variant G/A snv 40