Disease: Lymphocyte Count measurement
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs3732378
CX3CR1
0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 48
rs696
NFKBIA
0.708 0.520 14 35401887 3 prime UTR variant C/T snv 0.45 22
rs2229094
LOC100287329 ; LTA
0.776 0.320 6 31572779 missense variant T/C snv 0.27 0.27 17
rs11168249
HDAC7
0.807 0.120 12 47814585 intron variant T/C snv 0.50 9
rs2249742
HLA-B ; HLA-C
0.925 0.120 6 31272944 intron variant C/T snv 0.50 7
rs2524079
HLA-B
6 31274397 intron variant G/A snv 0.44 6
rs3735485
MYO1G
7 44969742 missense variant A/G snv 0.87 0.88 6
rs6475611 9 22151140 intergenic variant G/A snv 0.21 6
rs13063578
SETD2
3 47046347 intron variant T/A snv 0.46 5
rs34338164
PLEK
2 68388414 missense variant A/C snv 8.0E-03 7.8E-03 4
rs10411936
EPS15L1
1.000 0.080 19 16437564 intron variant A/G snv 0.63 3
rs10466905 12 6393666 upstream gene variant G/A snv 0.21 3
rs62237617
TTC28
22 28365160 intron variant C/G;T snv 1.9E-03 3
rs79716587
ARHGAP15
2 143129250 intron variant G/A snv 7.9E-02 3
rs10087240
PVT1
8 128000328 intron variant C/G;T snv 2
rs10422126
MIR24-2 ; MIR27A ; MIR23A ; LOC284454
19 13837498 non coding transcript exon variant G/A snv 0.37 2
rs1285886
RREB1
6 7140598 intron variant G/A snv 0.28 2
rs17041439
SPIC
12 101479462 intron variant A/C snv 7.0E-02 2
rs175714
LOC105370572
14 75515513 TF binding site variant T/C snv 0.50 2
rs1822534 3 12225304 intergenic variant A/G;T snv 2
rs1883932
LOC105372521 ; PLCB1
20 8628941 intron variant A/T snv 0.58 2
rs247826
MEAK7
16 84549359 intron variant C/T snv 0.18 2