Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12978472
INSR
19 7257979 intron variant C/G;T snv 5
rs13149993 4 80237391 regulatory region variant G/A;C snv 5
rs1573643
FURIN
15 90877743 intron variant T/C snv 0.33 5
rs167479
RGL3
19 11416089 missense variant T/A;C;G snv 5
rs16896398
SLC22A7
6 43294966 upstream gene variant A/T snv 0.42 5
rs1731249
KCNK3
2 26697157 intron variant T/A snv 0.48 5
rs2013002 12 111762346 intron variant T/A;C snv 5
rs2249105
CEP68
2 65060762 intron variant A/G snv 0.40 5
rs35441 12 115115310 intergenic variant C/T snv 0.40 5
rs35443 12 115115073 intergenic variant G/C snv 0.40 5
rs35444 12 115114632 intergenic variant A/G snv 0.38 5
rs3790604
WNT2B
1 112504257 intron variant C/A snv 7.8E-02 5
rs438885 2 164195781 intron variant A/T snv 0.56 5
rs4823006
ZNRF3
22 29055683 3 prime UTR variant A/G snv 0.41 5
rs4980389
LSP1
11 1871355 5 prime UTR variant G/A snv 0.35 5
rs5883070 7 27240226 intron variant -/AAAACA;AACA delins 0.91 5
rs6108787 20 10986566 intron variant T/G snv 0.46 5
rs62434109
PLEKHG1
6 150654176 intron variant T/G snv 8.4E-02 5
rs7125196
LOC105369329
11 61505093 intron variant T/C snv 0.16 5
rs7953257
HECTD4
12 112246417 intron variant A/G;T snv 0.71 5
rs79598313
KDF1
1 26958422 intron variant C/A;T snv 5
rs8068318
TBX2
17 61406405 non coding transcript exon variant C/T snv 0.56 5
rs9292468 5 32818967 intergenic variant T/A;C snv 5
rs10750766 11 65706327 regulatory region variant C/A snv 0.60 4
rs10766533
CSRP3 ; CSRP3-AS1
11 19203130 intron variant T/A snv 0.62 4