Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4807569
SBNO2
0.925 0.120 19 1123379 intron variant A/C snv 0.25 2
rs2024092
SBNO2
0.827 0.120 19 1124032 intron variant G/A snv 0.24 0.26 1
rs740495
SBNO2
1.000 0.040 19 1124836 intron variant A/C;G snv 1
rs4780355
SOCS1 ; RMI2 ; LOC105371082
0.882 0.120 16 11254001 intron variant T/C;G snv 2
rs367569
LOC105371082 ; RMI2
0.807 0.120 16 11271643 intron variant C/T snv 0.32 1
rs529866
LOC105371082 ; RMI2
1.000 0.040 16 11279463 intron variant C/T snv 0.18 1
rs6679677
PHTF1
0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 6
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 13
rs12552933 1.000 0.040 9 114759302 intergenic variant C/T snv 2.9E-02 1
rs4574921 0.882 0.160 9 114776054 upstream gene variant C/T snv 0.80 2
rs6478106 0.925 0.080 9 114783386 downstream gene variant C/T snv 0.34 2
rs10114470
TNFSF15
0.882 0.080 9 114785492 3 prime UTR variant T/A;C snv 2
rs10117785
TNFSF15
1.000 0.040 9 114789323 3 prime UTR variant T/A snv 0.34 1
rs3810936
TNFSF15
0.742 0.320 9 114790605 synonymous variant T/C snv 0.71 0.75 1
rs4246905
TNFSF15
0.716 0.400 9 114790969 missense variant T/A;C snv 0.76 2
rs6478108
TNFSF15
0.763 0.200 9 114796423 intron variant C/T snv 0.73 3
rs4372078
TNFSF15
1.000 0.040 9 114801407 intron variant T/G snv 0.78 1
rs4263839
TNFSF15
0.807 0.160 9 114804160 intron variant A/G snv 0.75 3
rs4979462
TNFSF15
0.790 0.240 9 114804733 intron variant C/T snv 0.13 2
rs6478109
TNFSF15
0.752 0.320 9 114806486 upstream gene variant A/G snv 0.74 2
rs7848647
TNFSF15
0.732 0.320 9 114806766 upstream gene variant T/C snv 0.74 1
rs7869487 0.882 0.040 9 114818634 intergenic variant C/G;T snv 1
rs2006996 0.882 0.080 9 114830358 regulatory region variant T/C snv 7.2E-02 3
rs16931910
DELEC1
1.000 0.040 9 114856029 intron variant A/C snv 7.2E-02 1
rs4979467
DELEC1
0.925 0.080 9 114867763 intron variant C/T snv 0.52 1