Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs79105258
CUX2
12 111280427 intron variant C/A;T snv 23
rs9942416 5 75741470 intergenic variant C/G snv 0.53 9
rs1495743 8 18415790 intergenic variant G/A;C snv 4
rs60808706
KCNQ1
11 2836003 intron variant G/A snv 0.12 4
rs11924032
SLC2A2
3 171017310 intron variant G/A snv 0.29 3
rs2232326
SPC25 ; G6PC2
2 168907981 missense variant T/C snv 5.1E-03 3.3E-03 3
rs2971672
GCK
7 44166307 intron variant A/C snv 0.44 3
rs61824877
LINC00862
1 200273504 intron variant G/A snv 0.11 3
rs9943291
HMGCS2
1 119749667 intron variant T/G snv 8.2E-02 3
rs10965246 9 22132699 downstream gene variant T/C snv 0.15 2
rs1203936 20 22611792 upstream gene variant G/C;T snv 2
rs12053049
SPC25
2 168910638 intron variant T/C snv 5.2E-02 2
rs12712928 2 44964941 intron variant G/C snv 0.18 2
rs1349497
RAPGEF4-AS1
2 172727935 intron variant G/A;C snv 2
rs1447352 11 92989595 downstream gene variant G/A snv 0.55 2
rs17277546
TRIM4
7 99891948 3 prime UTR variant G/A snv 3.1E-02 2
rs2411884
KCNQ1
11 2714304 intron variant C/A;G snv 2
rs4581570 13 27936575 intergenic variant T/A;C snv 2
rs477992
PHGDH
1 119714953 intron variant A/G snv 0.69 2
rs57884925
GLIS3
9 4285119 intron variant C/G;T snv 2
rs6975024
GCK
7 44192287 intron variant T/C snv 0.14 2
rs7200543
PDXDC1
16 15036113 synonymous variant A/G snv 0.35 0.30 2
rs76185967
RPL35P6 ; PSD3
8 18774816 non coding transcript exon variant C/T snv 1.6E-02 2
rs11185790
PANK1
10 89612776 intron variant G/A snv 0.15 1
rs12753193 1 65703996 non coding transcript exon variant G/A snv 0.58 1