Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 18
rs2820443 0.882 0.120 1 219580167 regulatory region variant T/C snv 0.23 8
rs9930333
FTO
0.882 0.120 16 53766065 intron variant T/C;G snv 5
rs2820436
LYPLAL1-AS1
0.882 0.040 1 219467338 intergenic variant A/C;G snv 4
rs3117582
BAG6 ; APOM
0.716 0.440 6 31652743 intron variant T/G snv 7.1E-02 3
rs532464664
CHADL
0.882 0.040 22 41238083 frameshift variant -/GCCCGCGC delins 4.8E-03 1.2E-02 3
rs2622873
COL11A1
0.882 0.040 1 103000497 intron variant T/C;G snv 3
rs4252548
IL11
1.000 0.040 19 55368304 missense variant C/T snv 2.1E-02 1.8E-02 3
rs10948172
SUPT3H ; LOC101929770
0.882 0.040 6 44809954 intron variant A/G snv 0.27 3
rs75621460
TGFB1
0.882 0.040 19 41327879 intron variant G/A snv 2.0E-02 3
rs10492367 0.882 0.040 12 27862037 regulatory region variant G/T snv 0.12 2
rs11997261 0.925 0.040 8 8666851 intron variant T/C;G snv 2
rs1913707 0.925 0.040 4 13037816 intergenic variant A/G snv 0.40 2
rs2785988 0.925 0.040 1 219570796 intergenic variant C/A snv 0.23 2
rs2847212 0.925 0.040 11 60568491 intergenic variant C/T snv 0.78 2
rs4979341 0.925 0.040 9 114143263 intergenic variant C/T snv 0.22 2
rs13283416
ASTN2 ; ASTN2-AS1
1.000 0.040 9 116539328 intron variant T/G snv 0.41 2
rs4836732
ASTN2 ; ASTN2-AS1
1.000 0.040 9 116504416 intron variant C/T snv 0.49 2
rs62406718
BTNL8
0.925 0.040 5 180923167 intron variant A/C;G snv 0.74 2
rs200975846
CCDC33
0.925 0.040 15 74325252 intron variant T/- delins 2
rs3753841
COL11A1
0.827 0.080 1 102914362 missense variant G/A snv 0.61 0.49 2
rs4144502
CRADD
0.925 0.040 12 93787552 intron variant G/A;C;T snv 2
rs11456119
DYNC1I1
0.925 0.040 7 96089185 intron variant A/-;AA;AAA delins 2
rs9977881
ERG
0.925 0.040 21 38635298 intron variant T/C;G snv 2
rs3884606
FGF18
0.925 0.040 5 171444070 intron variant G/A snv 0.54 2