Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2250417
BCO2
1.000 0.080 11 112214593 intron variant T/C snv 0.44 3
rs2599510
BIRC6
2 32600935 intron variant A/G snv 0.46 2
rs116383510 5 2545536 intergenic variant A/C snv 1.1E-02 1
rs116656892 5 68890201 intron variant T/C snv 1.5E-02 1
rs143253577 5 71806749 regulatory region variant G/A;C snv 1
rs144736172 2 31743073 intergenic variant A/G;T snv 1
rs4482818 4 65062779 intergenic variant A/C;G snv 1
rs71478720 11 112138882 intron variant C/T snv 0.16 1
rs2115763
BCO2
11 112180446 intron variant A/T snv 0.26 1
rs658805
COL19A1
6 70199369 intron variant G/A snv 0.34 1
rs1834481
IL18
0.882 0.160 11 112153104 non coding transcript exon variant C/G snv 0.16 1
rs10414578
LILRB1
19 54634619 non coding transcript exon variant C/G;T snv 4.5E-06; 0.11 1
rs4937291
LINC02762 ; LOC107984388
11 112340657 intron variant C/A;G;T snv 1
rs11124272
MEMO1 ; DPY30
2 31917451 intron variant C/A snv 0.28 1
rs192929104
MRPS36
5 69221046 intron variant G/A snv 6.5E-04 1
rs385076
NLRC4
2 32264782 5 prime UTR variant T/A;C snv 1
rs35082717
PTS
11 112239368 intron variant T/A;G snv 1
rs17229943
RAD17
5 69386709 intron variant A/C snv 4.1E-02 1
rs78623212
RELN
7 103667180 intron variant C/T snv 1.5E-02 1
rs6747488
SPAST
2 32086215 intron variant C/T snv 0.42 1
rs518600
SRD5A2
2 31629385 intergenic variant C/T snv 0.53 1
rs1979967
TMED3
15 79367271 intron variant C/T snv 0.25 1
rs2073316
XDH
2 31388163 intron variant G/A snv 0.42 1