Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6851943
LOC101929353
4 100203265 intron variant G/T snv 0.44 2
rs28470843
YY1 ; MIR6764
14 100276321 non coding transcript exon variant T/A;C snv 1
rs61993680
SLC25A29
14 100286307 intron variant A/C snv 0.39 1
rs11166440 1 100342807 upstream gene variant A/G;T snv 1
rs241812
SIM1 ; LOC102724406
6 100443115 intron variant A/G;T snv 2
rs1857859
SIM1
6 100446711 intron variant G/A snv 0.26 1
rs3775932
WDR1
4 10089306 intron variant C/A snv 0.47 1
rs1044261
GTPBP4 ; IDI2
1.000 0.080 10 1019770 stop gained C/T snv 5.0E-02 6.0E-02 3
rs17126268 1 102260843 intron variant T/C snv 7.3E-02 1
rs75174967
SUFU
10 102517336 intron variant G/A snv 8.2E-03 2
rs72995641 2 102549866 intergenic variant G/A snv 0.27 1
rs151134704
NFKB1 ; LOC105377347
4 102616435 splice region variant C/T snv 1.6E-04 9.1E-05 3
rs228611
MANBA
4 102640552 intron variant G/A snv 0.40 2
rs6833292 4 10270805 upstream gene variant C/T snv 0.44 1
rs223471
LOC102723704
4 102777629 intergenic variant G/C snv 0.38 1
rs284859
WBP1L
10 102813260 missense variant G/A;T snv 8.1E-06; 0.20 1
rs6892
WBP1L
10 102816113 3 prime UTR variant A/G snv 0.15 1
rs223401
UBE2D3
4 102817815 intron variant T/C snv 0.38 1
rs223308
CISD2 ; SLC9B1
4 102891342 3 prime UTR variant A/G snv 0.55 1
rs7688014
SLC9B2
4 103053903 intron variant T/C snv 0.65 1
rs200777151
SLC9B2
4 103057271 intron variant T/C snv 0.45 1
rs10715507
SLC9B2
4 103060542 intron variant TTTTTTT/-;T;TTTT;TTTTT;TTTTTT;TTTTTTTT;TTTTTTTTTT delins 1
rs1163087
INA
10 103283532 intron variant G/A snv 0.36 1
rs7832708
MSRA
8 10332530 intron variant C/T snv 0.49 4
rs11191686
PDCD11
10 103427989 intron variant G/A snv 0.29 1