Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11204896
RORC
1 151824266 intron variant C/G snv 7.6E-02 1
rs11217036 11 118805063 intergenic variant C/G;T snv 1
rs11236814
LINC02757
11 76632384 upstream gene variant A/T snv 0.13 1
rs11255968 10 8894199 upstream gene variant C/T snv 9.3E-02 1
rs11464691 17 40614389 intergenic variant -/A delins 0.68 1
rs1147169
PLCL1
2 198036671 intron variant T/C snv 0.67 1
rs11652139
PSMD3
17 39992780 intron variant G/A;C snv 1
rs11727978
TLR1
4 38809430 intron variant T/A snv 0.14 1
rs12045923
PEX14
1 10583772 intron variant C/G;T snv 1
rs12551834
KYAT1
9 128850912 intron variant G/A snv 7.4E-02 1
rs12596613
LOC400499
16 11397150 intron variant C/G snv 0.29 1
rs13088318
FAM172BP
3 101523907 downstream gene variant A/G;T snv 0.24 1
rs13153019 5 177355217 upstream gene variant T/C snv 0.21 1
rs13384448 2 227843146 intergenic variant C/T snv 0.67 1
rs13403656
SOCAR ; MIR4435-2HG
2 111511550 intron variant A/T snv 0.84 1
rs13437082 1.000 6 31386783 upstream gene variant C/T snv 0.32 1
rs1444789 10 9022398 intergenic variant T/C snv 0.23 1
rs150254607 4 122532955 intergenic variant -/TAT ins 4.9E-02 1
rs1505992 5 40498475 intron variant A/T snv 0.61 1
rs16899524
MICA-AS1
6 31394533 non coding transcript exon variant C/T snv 0.10 1
rs16922576
INSL6 ; JAK2
9 5064193 intron variant T/C snv 0.25 1
rs17607589
LPP
3 188684798 intron variant C/T snv 0.13 1
rs17664743 7 50214301 intron variant G/A snv 0.24 1
rs1775550 10 9010779 regulatory region variant G/A;C snv 1
rs1814576 5 110824180 intergenic variant T/C snv 7.0E-02 1