Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11074547
GRIN2A
16 10043032 intron variant T/G snv 0.32 1
rs2800281
TMEFF1 ; MSANTD3-TMEFF1
9 100572327 intron variant C/A;T snv 1
rs41310284 10 100687890 intergenic variant C/A;T snv 3
rs4780790
GRIN2A
16 10087779 intron variant G/T snv 0.68 1
rs4851541
IL1R1
2 102123999 intron variant G/T snv 0.40 1
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 24
rs9308315
LINC02456 ; IGF1
12 102410115 intron variant A/C;T snv 1
rs972936
IGF1 ; LINC02456
0.807 0.200 12 102431143 intron variant T/C snv 0.70 3
rs11191841
STN1
10 103879853 3 prime UTR variant T/C snv 0.47 3
rs17631425 2 104896266 intron variant A/C snv 0.68 1
rs370771
LIN28B
6 104950211 intron variant G/T snv 0.46 1
rs2252074
LINC01004 ; KMT2E
7 104953806 non coding transcript exon variant T/G snv 0.43 1
rs11097881 4 105127406 intergenic variant G/A snv 0.27 1
rs34161789
MYH2 ; MYHAS
17 10521326 missense variant C/T snv 4.1E-03 4.4E-03 1
rs11722225
INTS12 ; GSTCD
4 105845273 intron variant T/C snv 5.5E-02 3
rs146685629
INTS12
4 105854868 intron variant G/C snv 4.5E-02 1
rs34712979
NPNT
1.000 0.040 4 105897896 splice region variant G/A;T snv 0.17 5
rs2179687
SLX4IP
20 10633647 intron variant A/G snv 0.72 2
rs10157038
CASZ1
1 10652408 non coding transcript exon variant C/A;T snv 1
rs56890592 5 107326511 intergenic variant T/A snv 0.12 1
rs3764002
LOC105369965 ; WSCD2
1.000 0.080 12 108224853 missense variant C/T snv 0.27 0.20 3
rs893035
LOC101929621 ; RPL34-AS1
4 108557833 intron variant T/C snv 0.55 1
rs2802288
FOXO3
6 108575012 intron variant A/G snv 0.50 1
rs17034666
RANBP2 ; EDAR
2 108955052 intron variant G/A snv 0.11 1
rs7818891 8 109029943 intron variant G/A snv 0.62 1