Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10080237
BCKDHB
6 80144753 intron variant T/C snv 0.36 1
rs10101061
LOC107986930
8 23735787 intron variant T/A snv 0.30 1
rs10132280 14 25458973 intergenic variant C/A snv 0.37 6
rs10195252
COBLL1
0.925 0.080 2 164656581 intron variant T/C snv 0.48 6
rs10231365
ITGB8
7 20391962 intron variant C/T snv 0.57 1
rs10408163
ZC3H4
19 47093845 non coding transcript exon variant T/C snv 0.52 6
rs10429950 1.000 0.040 1 218451191 intergenic variant T/C snv 0.33 3
rs1043595
CALU
7 128769958 3 prime UTR variant G/A snv 0.19 2
rs1046934
TSEN15
1.000 0.080 1 184054395 missense variant A/C;G;T snv 0.34; 4.0E-06 2
rs10482795
TGFB2
1 218432267 intron variant G/A;T snv 2
rs10510554
RARB
3 25058285 intron variant T/C snv 0.53 2
rs1055144
LOC100506236
1.000 0.040 7 25831489 non coding transcript exon variant C/T snv 0.16 2
rs10786152
PLCE1
10 94133757 intron variant A/G snv 0.49 1
rs10804591 3 129615390 intergenic variant C/A snv 0.63 4
rs10842707 12 26318431 intron variant C/G;T snv 4
rs10842708 12 26321934 intron variant G/A snv 0.62 2
rs10843151
CCDC91
12 28318386 intron variant G/A snv 0.20 1
rs10849145
KCNA6 ; GALNT8 ; LOC105369614
12 4808002 intron variant T/C snv 0.15 1
rs10876528
HOXC6 ; HOXC5 ; HOXC4
12 54027692 intron variant C/A;G snv 2
rs10919388 1 170403362 intergenic variant A/C snv 0.71 4
rs10923712
TBX15
1 118962811 intron variant G/A snv 0.56 4
rs10923724 1 119004219 upstream gene variant C/T snv 0.53 3
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 8
rs10946808
H2AC9P
1.000 0.040 6 26233159 non coding transcript exon variant A/G snv 0.26 2
rs10968577
LINGO2
9 28415514 intron variant C/T snv 0.27 3