Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10430643
RNLS
10 88550323 intron variant T/A;C snv 0.45 1
rs1046276
CTF1
1.000 0.040 16 30903305 3 prime UTR variant T/C snv 0.62 2
rs10480300
PRKAG2
0.925 0.120 7 151708919 intron variant C/T snv 0.24 2
rs10483981
FLRT2
14 85653458 3 prime UTR variant C/T snv 0.27 1
rs10486757
GRB10
7 50626161 intron variant G/A snv 8.8E-02 1
rs10494964
LOC105372912
1 213793544 intron variant T/C snv 0.45 2
rs10495928
PRKCE
2 46126027 intron variant A/G snv 0.36 3
rs1050338
ZMIZ2
7 44768624 3 prime UTR variant G/A snv 0.39 1
rs1050828
G6PD
0.790 0.200 X 154536002 missense variant C/T snv 9.1E-03 3.6E-02 6
rs10517660
PDGFC
4 156921244 intron variant A/G snv 0.50 1
rs1052571
CASP9
0.882 0.080 1 15524118 missense variant G/A snv 0.50 0.59 1
rs1055253
BCAS1
20 53943587 3 prime UTR variant A/G snv 0.38 1
rs1058900
IFITM2
11 308290 missense variant T/C snv 0.70 0.70 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
rs1075871 3 194960568 regulatory region variant G/A snv 0.36 1
rs10761785
REEP3
10 63559006 intron variant G/T snv 0.51 3
rs10764671
ANKRD26
10 27095178 intron variant T/A;C snv 1
rs10766533
CSRP3 ; CSRP3-AS1
11 19203130 intron variant T/A snv 0.62 4
rs10767873
LOC101928338
11 30747131 intergenic variant C/T snv 0.35 2
rs10769263
SPI1
11 47395632 non coding transcript exon variant A/C snv 0.32 1
rs10772280
KLRC2
12 10428441 intron variant C/A;T snv 2
rs10774599 12 110259643 intergenic variant T/G snv 0.43 1
rs10774625
ATXN2
0.763 0.320 12 111472415 intron variant A/G snv 0.66 7
rs10779596 1 212903562 downstream gene variant G/T snv 0.61 1