Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs140859855
CRLF2
1.000 0.080 Y 1212602 synonymous variant G/A;C;T snv 1
rs1557055405
ABCD1
0.807 0.400 X 153743532 missense variant T/A snv 21
rs2407992
TLR8 ; TLR8-AS1
0.882 0.200 X 12920993 synonymous variant G/A;C snv 0.54 4
rs320995
CYSLTR1
0.851 0.240 X 78272820 missense variant G/A;C;T snv 0.73 4
rs2280964
CXCR3
0.882 0.200 X 71618204 intron variant C/A;G;T snv 3
rs2806489
CYSLTR1
1.000 0.080 X 78327951 upstream gene variant C/T snv 2
rs5953283
PPP1R3F
0.925 0.080 X 49283326 intron variant A/G;T snv 2
rs850637 0.925 0.080 X 13005622 intergenic variant G/A snv 0.43 2
rs12007907
IL1RAPL1
1.000 0.080 X 29465775 intron variant C/A snv 0.12 1
rs738409
PNPLA3
0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs1034395178
LZTR1
0.716 0.480 22 20996071 stop gained C/A;T snv 4.0E-06; 8.0E-06 33
rs2284033
IL2RB
0.790 0.160 22 37137994 intron variant G/A snv 0.43 7
rs10048897
LINC00528
1.000 0.080 22 17777938 non coding transcript exon variant T/C snv 9.9E-02 1
rs138335
ST13
1.000 0.080 22 40831082 intron variant C/A;G snv 1
rs138337
ST13
1.000 0.080 22 40835049 intron variant A/G snv 0.46 1
rs5758364
PHF5A
1.000 0.080 22 41459908 3 prime UTR variant A/C;T snv 1
rs9620247 1.000 0.080 22 23333616 intergenic variant G/A snv 3.9E-02 1
rs1202989817
SOD1 ; LOC102724449
0.716 0.360 21 31659813 missense variant T/C;G snv 8.0E-06 7.0E-06 18
rs4819388
ICOSLG
0.790 0.240 21 44227538 3 prime UTR variant T/C snv 9
rs1736135
LOC101927745
0.851 0.160 21 15432901 intron variant T/C snv 0.33 4
rs762421
GATD3A
0.851 0.360 21 44195678 intron variant G/A snv 4
rs11088309
RUNX1
0.925 0.080 21 35092334 intron variant C/A;G snv 9.3E-02 2
rs2012075
IFNGR2
1.000 0.080 21 33424455 intron variant C/G;T snv 1
rs2834787
RUNX1
1.000 0.080 21 35130261 intron variant A/G snv 0.15 1
rs7281353
LINC01425
1.000 0.080 21 21779123 intron variant C/G snv 0.76 1