Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12741980 1 11879536 non coding transcript exon variant A/C snv 5.8E-02 2
rs12958173
LINC01478
18 44562012 intron variant A/C snv 0.70 2
rs17245822 13 72557556 intergenic variant A/C snv 0.34 2
rs2289125
NOX4
11 89491285 5 prime UTR variant A/C snv 0.69 0.61 2
rs259983
ZNF831
20 59160402 5 prime UTR variant A/C snv 0.25 2
rs28663144
SVEP1
9 110436611 intron variant A/C snv 4.9E-02 2
rs6090040
TCEA2
20 64060707 intron variant A/C snv 0.52 2
rs6565174
LOC101928595
16 30100583 intron variant A/C snv 0.93 2
rs7297416
HOXC4
12 54049306 intron variant A/C snv 0.34 2
rs75460349
ZDHHC18
1 26853597 intron variant A/C snv 1.7E-02 2
rs76326501
LOC105374567 ; LOC112268413
2 42940738 intergenic variant A/C snv 5.7E-02 2
rs7665304
LEF1
4 108104223 intron variant A/C snv 0.53 2
rs8105753 19 31436641 regulatory region variant A/C snv 0.33 2
rs954767 5 3705936 intergenic variant A/C snv 0.27 2
rs9969423
FAM167A-AS1
8 11398066 intron variant A/C snv 0.39 2
rs10143078
COX16 ; SYNJ2BP-COX16 ; SYNJ2BP
14 70414772 intron variant A/C snv 6.6E-02 1
rs10203824 2 190731124 intergenic variant A/C snv 0.22 1
rs10429910
ZBTB41
1 197172123 intron variant A/C snv 0.28 0.21 1
rs10876531
HOXC4
12 54049934 intron variant A/C snv 0.34 1
rs11125883
XPO1
2 61483438 non coding transcript exon variant A/C snv 0.31 1
rs11154334
NCOA7
6 125893478 intron variant A/C snv 0.30 1
rs11228620
MYEOV
11 69306875 intron variant A/C snv 0.26 1
rs11672460
GNG7
19 2588425 intron variant A/C snv 1.5E-02 1
rs117874826
PLCB3
11 64260194 missense variant A/C snv 7.8E-03 9.4E-03 1
rs12088448
TGFB2
1 218372828 intron variant A/C snv 0.43 1