Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2071449
HOXC4 ; HOXC5 ; MIR615
12 54034227 intron variant C/A;T snv 0.35; 4.2E-06 4
rs2156552
LOC105372112
1.000 0.040 18 49655298 downstream gene variant A/G;T snv 4
rs2392929 7 106773623 upstream gene variant T/A;C;G snv 4
rs34071855
CASZ1
1 10738432 intron variant C/G;T snv 4
rs41274050
ASAH2B ; A1CF
10 50814012 missense variant C/A;T snv 4.0E-06; 5.3E-03 4
rs4722551
LOC105375199
7 25952206 upstream gene variant T/C;G snv 4
rs4759319
HOXC4 ; HOXC6 ; HOXC5
12 54030947 intron variant G/C;T snv 4
rs4820323
MAFF ; PLA2G6
22 38203760 non coding transcript exon variant C/A;G;T snv 4
rs60695258
AFF1
4 87101557 intron variant C/A;T snv 4
rs640065
NEK10
3 27322446 intron variant T/A;C snv 4
rs7185735
FTO
0.925 0.120 16 53788739 intron variant A/G;T snv 4
rs72831345
CABCOCO1
10 61758990 intron variant G/A;C snv 4
rs8071884
PGS1
17 78401977 intron variant C/A;G;T snv 4
rs10826334 10 59620724 intron variant C/A;G snv 3
rs112640876
LSP1
11 1873813 intron variant A/G;T snv 3
rs13280442 8 11610048 intergenic variant C/A;G snv 3
rs2004776
AGT
1 230712956 intron variant C/G;T snv 3
rs2304128
GMIP
19 19635342 intron variant G/C;T snv 3
rs2493141
LOC105373166
1 230729374 intron variant G/A;T snv 3
rs2586886
KCNK3
1.000 0.080 2 26709163 intron variant C/G;T snv 3
rs287
LPL
8 19958045 intron variant A/G;T snv 3
rs2963472 5 158572014 intron variant G/A;C snv 3
rs3753581
NPPB
1 11860132 upstream gene variant C/A;T snv 3
rs3794695
HPR ; TXNL4B
16 72063928 intron variant C/A;T snv 3
rs4475251 5 115039988 intergenic variant G/A;T snv 3