Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2294239
ZNRF3
22 29053489 intron variant A/G snv 0.36 4
rs2316205 19 40840863 non coding transcript exon variant T/C snv 0.40 4
rs2645294
WARS2
1 119031964 3 prime UTR variant C/T snv 0.59 4
rs6012558 20 48914749 intergenic variant G/A snv 0.42 4
rs7162542
ADAMTSL3
15 83845538 intron variant C/A;G;T snv 4
rs7970350
HMGA2
12 65966384 downstream gene variant C/T snv 0.48 4
rs8010717
LOC107984630
14 79944098 intron variant T/C snv 0.29 4
rs8066985 17 70457204 intergenic variant A/G snv 0.56 4
rs9435732
MFAP2
1 16981663 intron variant C/G;T snv 4
rs10245353 7 25818994 intergenic variant C/A snv 0.16 3
rs1106529
TBX15
1 118988874 intron variant G/A snv 0.77 3
rs113029345 19 40864271 intron variant T/C snv 3
rs117582141 10 92804854 intergenic variant T/A;C snv 3
rs12317176
CCDC92 ; DNAH10
12 123920171 intron variant T/C snv 0.39 3
rs12493901
FNDC3B
3 172204265 intron variant G/A snv 0.37 3
rs12608504 19 18278325 upstream gene variant A/G;T snv 3
rs12692737
COBLL1
2 164697799 non coding transcript exon variant C/A snv 0.42 3
rs12731372 1 118310352 regulatory region variant C/T snv 0.19 3
rs1294410
LOC101928004
6 6738519 intron variant T/C snv 0.65 3
rs12991495
DNMT3A
2 25263901 intron variant T/C snv 0.22 3
rs13083798
PBRM1
3 52615732 intron variant A/G snv 0.51 3
rs1385167
LOC105369168
2 65973514 intron variant A/G snv 0.18 3
rs1534696
SNX10
7 26357619 intron variant C/A snv 0.58 3
rs1569135
LOC105373786
2 187250671 intron variant A/G snv 0.51 3
rs17396340
KIF1B
1 10226118 intron variant G/A;C snv 3