Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs60317590
LOC105370809
15 48651693 non coding transcript exon variant TTTTTTTTTTTT/-;TTTTTTT;TTTTTTTT;TTTTTTTTT;TTTTTTTTTT;TTTTTTTTTTT;TTTTTTTTTTTTT;TTTTTTTTTTTTTT;TTTTTTTTTTTTTTT delins 1
rs34846688
STAT3
17 42343456 intron variant TTTTTTTTTTTT/-;T;TT;TTT;TTTTT;TTTTTT;TTTTTTT;TTTTTTTT;TTTTTTTTT;TTTTTTTTTT;TTTTTTTTTTT;TTTTTTTTTTTTT;TTTTTTTTTTTTTT;TTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTT delins 0.30 1
rs201851995
RSRC1
3 158119720 intron variant TTAT/- delins 1.4E-04 2
rs565853247 4 80247467 intergenic variant TT/-;T;TTT delins 1
rs3063286
SLX4IP
20 10507905 intron variant TA/-;TATA;TATATA;TATATATA;TATATATATA delins 1
rs78378222
TP53
0.662 0.360 17 7668434 3 prime UTR variant T/G snv 8.3E-03 15
rs6108787 20 10986566 intron variant T/G snv 0.46 5
rs62434109
PLEKHG1
6 150654176 intron variant T/G snv 8.4E-02 5
rs11105364
ATP2B1
12 89675499 intron variant T/G snv 0.15 4
rs569550
LSP1
0.925 0.080 11 1865838 intron variant T/G snv 0.35 4
rs7483477
LINC01150
11 1899025 intron variant T/G snv 0.25 4
rs1544935 0.925 0.160 6 39156672 intergenic variant T/G snv 0.18 3
rs453301 8 9172877 intron variant T/G snv 0.54 3
rs6669371
CLCN6
1 11822085 intron variant T/G snv 0.14 3
rs925946
BDNF-AS
0.882 0.120 11 27645655 intron variant T/G snv 0.72 3
rs9810888
CACNA1D
3 53601568 intron variant T/G snv 0.51 3
rs12209106 6 1620807 downstream gene variant T/G snv 0.37 2
rs13008299
TOGARAM2
2 29025131 intron variant T/G snv 0.28 2
rs7535162
SDCCAG8
1 243262387 intron variant T/G snv 0.28 2
rs10078021 5 75742606 intergenic variant T/G snv 0.51 1
rs10164193
ASXL3
18 33581462 intron variant T/G snv 0.13 1
rs10193543
EXOC6B
2 72256200 intron variant T/G snv 0.13 1
rs12142296
P3R3URF-PIK3R3 ; PIK3R3
1 46076007 intron variant T/G snv 9.7E-02 1
rs12216886
VLDLR-AS1 ; LOC101930053
9 2493751 intron variant T/G snv 0.18 1
rs148772934 11 44984130 regulatory region variant T/G snv 3.8E-04 1