Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10006235
LINC02466
1.000 0.040 4 129748953 non coding transcript exon variant T/C snv 0.73 2
rs10012947 1.000 0.040 4 30491805 regulatory region variant C/T snv 0.33 1
rs10046758
CSMD1
1.000 0.040 8 4326648 non coding transcript exon variant C/G;T snv 1
rs10061788
LINC00461
1.000 0.040 5 88638889 intron variant G/A;T snv 2
rs1006737
CACNA1C
0.695 0.120 12 2236129 intron variant G/A snv 0.36 5
rs10074991
PRKAA1
0.851 0.120 5 40790449 intron variant G/A snv 0.31 2
rs10077591 1.000 0.040 5 165935005 intergenic variant C/T snv 0.44 1
rs1008078 1.000 0.040 1 90724174 non coding transcript exon variant C/T snv 0.33 2
rs10083370
LINC00637 ; PPP1R13B
1.000 0.040 14 103847845 intron variant G/A snv 0.55 1
rs10085567
GTF2IP7
1.000 0.040 7 76104888 intron variant A/C snv 0.43 1
rs10098073
TSNARE1
1.000 0.040 8 142228143 intron variant C/A snv 0.35 1
rs10124101
LOC102724322
1.000 0.040 9 36308830 upstream gene variant G/A snv 0.53 1
rs10148671
LINC02326
1.000 0.040 14 29000167 intron variant T/C snv 0.51 1
rs10156310
NSD3
1.000 0.040 8 38351611 intron variant A/C;G;T snv 1
rs10180106
CTNNA2
1.000 0.040 2 79994772 intron variant G/A snv 0.22 1
rs10196799
ZNF804A
1.000 0.040 2 184776001 intron variant A/T snv 0.34 1
rs10199182
LINC01830 ; LINC01884
1.000 0.040 2 22524252 intron variant A/G;T snv 1
rs10204454 1.000 0.040 2 193481559 intergenic variant C/T snv 0.44 1
rs10204933 1.000 0.040 2 228206898 intergenic variant A/G snv 0.15 1
rs10211550
MOB4 ; HSPE1-MOB4
1.000 0.040 2 197518575 intron variant G/T snv 0.37 2
rs1021487 1.000 0.040 4 58590920 intergenic variant T/C snv 0.15 1
rs1023500
CENPM
1.000 0.040 22 41944840 intron variant T/C snv 0.27 1
rs1024582
CACNA1C
1.000 0.040 12 2293080 intron variant A/G;T snv 2
rs10272006
SP4
0.925 0.080 7 21480514 intron variant G/A snv 0.75 2
rs10275045
MAD1L1
0.882 0.160 7 1881190 intron variant C/T snv 0.35 2