Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10008032
LOC105374413
1.000 0.080 4 38743861 intergenic variant T/C snv 0.66 2
rs10008637
SHROOM3
4 76492991 intron variant T/A;C snv 0.35 2
rs10009128 0.925 0.040 4 19511508 intron variant C/T snv 0.34 2
rs10009397 4 28695228 intergenic variant A/T snv 0.89 1
rs1000940
RABEP1 ; NUP88
17 5379957 intron variant A/G snv 0.31 1
rs10009409
LOC105377273 ; LOC107986286
1.000 0.080 4 72989536 intergenic variant C/T snv 0.35 1
rs10009715
LOC105377535
4 171510209 intron variant T/A;C snv 1
rs1000972 20 6641070 regulatory region variant T/A;G snv 2
rs1001007
CCR5AS
0.827 0.120 3 46387167 intron variant A/G;T snv 5
rs10010325
TET2 ; TET2-AS1
1.000 0.040 4 105185196 intron variant C/A;G;T snv 3
rs10010954
LRBA
1.000 0.040 4 150324302 intron variant T/A;C snv 1
rs1001096
ART4 ; C12orf60
12 14835521 intron variant G/A snv 0.32 1
rs10011007 4 130143535 intergenic variant A/C snv 8.3E-02 1
rs10011263
ANK2
1.000 0.040 4 112807837 intergenic variant G/A snv 0.22 1
rs10011796
ABCG2
0.882 0.160 4 88169725 intron variant T/C;G snv 3
rs10011838 1.000 0.080 4 152599127 intergenic variant G/A snv 0.42 3
rs10012282
WDR17
1.000 0.080 4 176155096 intron variant T/C;G snv 5.2E-02 1
rs10012488
INPP4B
1.000 0.040 4 142671933 intron variant C/T snv 7.7E-02 1
rs10012947 1.000 0.040 4 30491805 regulatory region variant C/T snv 0.33 1
rs10013696
TBC1D14
4 6977000 intron variant A/G snv 0.45 1
rs1001494
ST7L
1 112567997 intron variant T/C snv 0.50 1
rs10015415
FAM13A
4 89007052 intron variant T/C snv 0.54 2
rs10015974
WWC2
4 183275101 intron variant A/G;T snv 1
rs10016631
POLR2B
4 57019797 intron variant A/G;T snv 1
rs10016841
LOC105374514
4 20212158 intergenic variant T/C snv 0.16 1