Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1032129
TNFRSF11B
0.851 0.040 8 118939661 intron variant A/C snv 0.37 5
rs11073337
RASGRP1
0.851 0.040 15 38555562 intron variant A/C snv 0.27 5
rs1199047
CCDC88B
0.882 11 64350711 intron variant A/C snv 0.38 4
rs1921445 0.882 3 106229671 intergenic variant A/C;G snv 4
rs11145763
CARD9
0.724 0.240 9 136369144 intron variant A/C;G;T snv 14
rs391851 0.882 5 103342219 intergenic variant A/C;G;T snv 4
rs8061370
LOC105371082 ; RMI2
0.882 16 11364614 intron variant A/C;T snv 4
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 34
rs4625
DAG1
0.716 0.280 3 49534707 3 prime UTR variant A/G snv 0.30 17
rs12598357 0.724 0.240 16 28329624 intergenic variant A/G snv 0.43 15
rs17466626
LOC105369736 ; LRRK2
0.724 0.240 12 40366829 non coding transcript exon variant A/G snv 1.7E-02 14
rs72743477
SMAD3
0.724 0.240 15 67171953 intron variant A/G snv 0.17 14
rs1893217
PTPN2
0.742 0.440 18 12809341 intron variant A/G snv 0.12 10
rs10425559 0.807 0.040 19 4837475 upstream gene variant A/G snv 0.66 7
rs7441808
LINC02357
0.851 0.040 4 26088753 intron variant A/G snv 0.20 5
rs12980063
CPT1C
0.882 19 49693735 intron variant A/G snv 0.48 4
rs1320344
C12orf42
0.882 12 103493699 intron variant A/G snv 0.64 4
rs4761587
PLXNC1
0.882 12 94158023 intron variant A/G snv 0.78 4
rs56817615
CLNK
0.882 4 10717222 intergenic variant A/G snv 0.42 4
rs9683415 0.882 4 40290296 regulatory region variant A/G snv 0.71 4
rs761357
LINC00271
0.851 0.040 6 135581461 intron variant A/G;T snv 5
rs221781 0.882 7 100698285 upstream gene variant A/G;T snv 4
rs773107
RAB5B
0.882 12 55975722 intron variant A/G;T snv 4
rs55984493 0.851 0.040 13 99118074 intergenic variant A/T snv 0.15 5
rs10986284 0.882 9 124236874 intergenic variant A/T snv 0.27 4