Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121908120
WNT10A
0.701 0.280 2 218890289 missense variant T/A snv 1.4E-02 1.4E-02 11
rs77542162
ABCA6
1.000 0.040 17 69085137 missense variant A/G snv 9.3E-03 1.0E-02 10
rs6795735
ADAMTS9-AS2
0.882 0.120 3 64719689 intron variant C/A;G;T snv 6
rs61816761
FLG ; FLG-AS1
0.658 0.640 1 152313385 stop gained G/A;T snv 9.4E-03; 8.0E-06 5
rs1536482 1.000 0.040 9 134548682 upstream gene variant G/A snv 0.36 2
rs2721051 1.000 0.040 13 40536747 intron variant C/T snv 8.6E-02 2
rs9938149 0.925 0.160 16 88298034 intron variant C/A snv 0.66 2
rs5749482
LOC105373002 ; SYN3
0.925 0.040 22 32663679 intron variant G/C snv 0.26 2
rs4954218
MAP3K19
0.925 0.080 2 135045855 intron variant G/T snv 0.83 2
rs1324183 1.000 0.040 9 13557492 intron variant A/C;T snv 1
rs8111998 1.000 0.040 19 22558873 downstream gene variant C/T snv 0.23 1
rs7044529
COL5A1
1.000 0.040 9 134676205 intron variant C/T snv 0.21 1
rs4894535
FNDC3B
1.000 0.040 3 172277815 intron variant C/A;T snv 1
rs1143627
IL1B
0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56 1
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 1
rs1052536
LIG3
0.776 0.200 17 35004556 3 prime UTR variant C/T snv 0.42 0.36 1
rs1800449
LOX
0.641 0.400 5 122077513 missense variant C/A;T snv 4.0E-06; 0.17 1
rs61752717
MEFV
0.583 0.840 16 3243407 missense variant T/A;C snv 2.8E-04 1
rs6430585
UBXN4
1.000 0.040 2 135749357 intron variant A/C snv 0.74 1