Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9371601
SYNE1
0.790 0.120 6 152469438 intron variant G/T snv 0.46 6
rs2388334 0.882 0.040 6 98143746 intron variant A/G snv 0.39 5
rs9834970 0.790 0.080 3 36814539 downstream gene variant T/C snv 0.45 3
rs78381888
ANKRD23 ; CNNM3
0.925 0.040 2 96835038 3 prime UTR variant A/G snv 0.13 3
rs55648125 0.925 0.040 6 50849005 downstream gene variant A/G snv 7.9E-02 2
rs57681866 0.925 0.040 2 57748579 intergenic variant G/A snv 6.4E-02 2
rs73496688 0.925 0.040 11 79445704 upstream gene variant T/A snv 0.15 2
rs10994318
ANK3
0.925 0.040 10 60366098 intron variant G/C snv 7.3E-02 2
rs10744560
CACNA1C ; CACNA1C-IT3
0.882 0.040 12 2277933 intron variant C/G;T snv 2
rs4301023
CADM2
0.925 0.040 3 85008130 intron variant C/T snv 0.51 2
rs12226877
FADS2 ; FADS1
0.925 0.040 11 61824435 intron variant G/A snv 0.14 2
rs11647445
GRIN2A
0.925 0.040 16 9833109 intron variant T/G snv 0.35 2
rs10058613
KDM3B
0.925 0.040 5 138358306 intron variant C/A;G;T snv 2
rs10745843
LOC101928937 ; ANKS1B
0.925 0.040 12 99102252 intron variant G/A snv 0.55 2
rs6090435
LOC105372725
0.925 0.040 20 63501358 upstream gene variant G/A snv 0.38 2
rs4794820
LRRC3C
0.790 0.160 17 39933091 intron variant A/G;T snv 2
rs111444407
NCAN
0.925 0.040 19 19247398 intron variant C/T snv 0.24 2
rs57957974
PARP10
0.925 0.040 8 144002361 intron variant C/A snv 0.30 2
rs138321
SLC25A17
0.925 0.040 22 40813300 intron variant G/A snv 0.51 2
rs10147900 1.000 0.040 14 104625694 intergenic variant C/T snv 0.17 1
rs11972012 1.000 0.040 7 44946070 intergenic variant C/G;T snv 1
rs1331621 1.000 0.040 9 119412084 intergenic variant T/A;C snv 1
rs17395886 1.000 0.040 4 161358233 intergenic variant C/A;G snv 1
rs2052387 1.000 0.040 12 68483007 upstream gene variant A/C snv 0.72 1
rs56158970 1.000 0.040 7 115282097 intergenic variant A/G snv 1.1E-02 1