Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1046411
CNNM2
10 103078059 3 prime UTR variant G/A snv 0.32 1
rs1047891
CPS1
0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 25
rs1048310
ATF4 ; MIEF1
22 39517277 3 prime UTR variant T/G snv 0.32 1
rs1049212
PPL
16 4882928 3 prime UTR variant A/G snv 0.43 1
rs10495161 1 220963330 regulatory region variant C/T snv 0.14 1
rs10496344
AFF3
2 100147663 intron variant T/C;G snv 1
rs1050828
G6PD
0.790 0.200 X 154536002 missense variant C/T snv 9.1E-03 3.6E-02 6
rs10510562
RARB
3 25340465 intron variant G/C snv 0.23 1
rs1064351
HOMER3 ; HOMER3-AS1
19 18938389 synonymous variant G/A snv 0.40 0.34 1
rs10736831
TMEM72-AS1
10 44906863 intron variant G/A snv 0.55 2
rs10750385 11 128067871 regulatory region variant A/C;G snv 0.76 1
rs10758656
RCL1
9 4852599 intron variant A/G snv 0.19 6
rs10758658
RCL1
9 4856877 intron variant G/A snv 0.15 3
rs10762861 10 79377440 upstream gene variant A/G snv 0.80 1
rs10766471
GTF2H1
11 18345583 intron variant C/T snv 0.45 1
rs10766533
CSRP3 ; CSRP3-AS1
11 19203130 intron variant T/A snv 0.62 4
rs10772280
KLRC2
12 10428441 intron variant C/A;T snv 2
rs10783487
ATG101
12 52068035 upstream gene variant G/A;T snv 2
rs10786774
STN1
10 103884565 intron variant G/C snv 0.90 1
rs1078859
LYST
1 235748725 intron variant C/A snv 0.26 1
rs10793565
TMEM72-AS1
10 44892783 intron variant G/C snv 0.53 2
rs10801682
PKN2
1 88708570 intron variant A/T snv 0.50 1
rs10833106
NAV2
11 19401081 intron variant A/G snv 0.19 1
rs10846742
SCARB1
12 124824136 intron variant G/A;T snv 2
rs10849020 12 4222843 intergenic variant C/G snv 0.22 2