Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7200786
CLEC16A
0.882 0.200 16 11083944 intron variant A/G snv 0.59 2
rs12708716
CLEC16A
0.807 0.320 16 11086016 intron variant A/G snv 0.37 4
rs12927355
CLEC16A
0.882 0.240 16 11100914 intron variant C/A;T snv 0.29 2
rs998592
CLEC16A
0.925 0.160 16 11105821 intron variant C/T snv 0.39 1
rs7184083
CLEC16A ; LOC105371081
1.000 0.080 16 11134057 intron variant A/G snv 0.72 1
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 24
rs2903692
CLEC16A
0.807 0.360 16 11144926 intron variant G/A snv 0.33 1
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 17
rs17174870
MERTK
1.000 0.080 2 111907624 intron variant C/T snv 0.24 1
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30 11
rs4807569
SBNO2
0.925 0.120 19 1123379 intron variant A/C snv 0.25 2
rs12928822
LOC105371082 ; RMI2
0.882 0.200 16 11310036 intron variant C/T snv 0.13 5
rs7191700
RMI2 ; LOC105371082
1.000 0.080 16 11312946 intron variant C/T snv 0.27 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
rs4263839
TNFSF15
0.807 0.160 9 114804160 intron variant A/G snv 0.75 3
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 7
rs13277113
BLK
0.695 0.520 8 11491677 intron variant G/A snv 0.25 2
rs12025416
LOC112268235
1.000 0.080 1 116495665 intron variant T/A;C snv 1
rs1335532
CD58
1.000 0.080 1 116558335 intron variant A/G snv 0.28 1
rs2300747
MIR548AC ; CD58
0.882 0.200 1 116561593 intron variant A/G snv 0.19 1
rs11586238 0.925 0.160 1 116720516 regulatory region variant C/G snv 0.19 4
rs1801131
MTHFR
0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 1
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 3
rs630923
CXCR5
1.000 0.080 11 118883644 upstream gene variant C/A snv 0.13 2