Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10431386
MLEC
1.000 0.040 12 120691123 intron variant C/T snv 0.34 1
rs1057519583
STN1
0.882 0.160 10 103900115 missense variant C/G snv 1
rs1060499939
SPAST
0.882 0.120 2 32137172 missense variant G/C;T snv 4
rs1131692230
PDHA1
0.807 0.160 X 19353124 missense variant A/G snv 9
rs121918399
APOE
0.925 0.120 19 44907843 missense variant C/T snv 8.0E-06 1
rs121918455
PTPN11
0.695 0.440 12 112477720 missense variant A/C;G snv 31
rs1345176461
LOC107984638 ; IRF2BPL
0.716 0.240 14 77027231 stop gained G/A;T snv 4.3E-06 40
rs1476413
MTHFR
0.790 0.360 1 11792243 intron variant C/G;T snv 4.0E-06; 0.26 0.23 1
rs1553630279
CTNNB1
0.807 0.160 3 41225049 stop gained C/T snv 7
rs1554208945
ZNF292
0.752 0.240 6 87260207 missense variant A/C snv 26
rs1555247672
MED13L
0.827 0.200 12 116007542 stop gained G/A snv 14
rs1555303073
COL4A1
0.851 0.120 13 110176912 missense variant C/T snv 6
rs1555377415
IRF2BPL ; LOC107984638
0.827 0.200 14 77027274 stop gained G/C snv 18
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 1
rs1799724
LTA ; TNF
0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 2
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 1
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 2
rs1801131
MTHFR
0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 1
rs2069837
IL6-AS1 ; IL6
0.724 0.520 7 22728408 intron variant A/C;G snv 2
rs2853749
SPP1
0.882 0.160 4 87976662 intron variant C/T snv 0.34 2
rs28934906
MECP2
0.716 0.320 X 154031355 missense variant G/A snv 40
rs28936415
PMM2
0.752 0.320 16 8811153 missense variant G/A snv 4.1E-03 3.7E-03 22
rs3024490
IL10 ; IL19
0.742 0.520 1 206771966 intron variant A/C;G;T snv 1
rs405509
APOE
0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58 9
rs429358
APOE
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 29