Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs74847330
ARHGAP15
2 143074030 intergenic variant A/G snv 8.8E-02 4
rs1057258
INPP5D
2 233206983 3 prime UTR variant C/T snv 0.30 3
rs11684176
PLCL1
2 198090050 intron variant C/T snv 0.38 3
rs1595824
PLCL1
2 198009282 intron variant C/A;T snv 3
rs346835
LINC00299
2 8298563 intron variant C/T snv 0.39 3
rs4850808 2 197711418 intron variant T/A;C snv 3
rs6021268
NFATC2
20 51524602 intron variant T/C snv 5.8E-02 3
rs697852
ITPKB
1 226727033 intron variant G/A snv 0.82 3
rs9889262
ZNF652
17 49320708 intron variant T/A snv 0.28 3
rs1064213
PLCL1
2 198085516 missense variant G/A snv 0.44 0.41 2
rs1147169
PLCL1
2 198036671 intron variant T/C snv 0.67 2
rs12522383
WDR36
5 111119568 intron variant G/A snv 0.29 2
rs1505992 5 40498475 intron variant A/T snv 0.61 2
rs16899524
MICA-AS1
6 31394533 non coding transcript exon variant C/T snv 0.10 2
rs17496549
HLA-DRA
6 32441931 intron variant C/T snv 0.10 2
rs1997502
IL1RL2
2 102227789 intron variant A/G;T snv 2
rs2030520
LPP
3 188401794 intron variant C/G;T snv 2
rs2095044 9 6192796 upstream gene variant T/C snv 0.64 2
rs2134814
BACH2
6 90277793 intron variant C/G snv 0.26 2
rs2197415 10 9020893 intergenic variant T/G snv 0.66 2
rs2294882
TSBP1-AS1 ; BTNL2
6 32399738 intron variant T/C snv 0.19 2
rs3540
IQGAP1
15 90502176 3 prime UTR variant G/A snv 0.43 2
rs4851005
IL18R1
2 102395092 intron variant C/T snv 0.29 2
rs6011033
RTEL1-TNFRSF6B ; RTEL1
20 63691346 intron variant A/G;T snv 2
rs616402
PEX14
1 10506215 intron variant C/T snv 0.29 2