Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1047743
UNK
17 75794012 3 prime UTR variant C/G;T snv 1
rs10490120 2 48916690 intron variant A/G snv 9.3E-02 1
rs10490626
LOC107985940
2 118078265 intergenic variant G/A snv 5.2E-02 2
rs10513551
TRIM59-IFT80 ; IFT80
3 160368267 intron variant G/T snv 0.53 1
rs1065853 19 44909976 non coding transcript exon variant G/A;C;T snv 4
rs10744775
BRAP
12 111658411 intron variant T/C snv 0.44 2
rs10761716 10 63122540 downstream gene variant C/G snv 0.40 3
rs10764055
PCAT5
10 35777511 upstream gene variant T/A;G snv 1
rs10808546 8 125483576 intron variant C/T snv 0.39 6
rs10832027
ARNTL
11 13335636 intron variant G/A snv 0.67 5
rs10832961
SPTY2D1
11 18632410 intron variant C/G;T snv 2
rs10876041
DIP2B
12 50508099 intron variant T/C snv 0.58 4
rs10885997
PNLIPRP2
10 116638460 synonymous variant A/G snv 0.38 0.36 2
rs10889348
DOCK7
1 62612551 intron variant A/T snv 0.32 3
rs10889353
DOCK7
1 62652525 intron variant A/C;T snv 4
rs10893499
ST3GAL4
11 126372084 intron variant G/A snv 0.16 2
rs10900522
NUCKS1
1 205714939 3 prime UTR variant T/C snv 0.21 4
rs10903129
MACO1
1 25442446 intron variant A/G snv 0.58 3
rs10957054
UBXN2B
8 58423997 intron variant C/T snv 0.73 3
rs11024735
SPTY2D1
11 18617620 intron variant C/G;T snv 2
rs11048456
LOC105369705
1.000 0.080 12 26310149 intron variant C/T snv 0.62 6
rs11065987 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 10
rs11079810
SKAP1
17 48150484 intron variant C/T snv 0.16 4
rs11080150
NF1
17 31302308 intron variant A/G snv 0.36 2
rs11136341
PLEC
8 143969375 intron variant A/G snv 0.40 2