Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10426401
LOC107985305 ; PVR
1.000 0.080 19 44644419 intron variant T/G snv 0.32 2
rs10438978
LOC105372112
18 49631816 intergenic variant T/C snv 0.75 2
rs1045241
TNFAIP8
1.000 0.120 5 119393591 3 prime UTR variant C/T snv 0.30 5
rs10468017
ALDH1A2
0.851 0.120 15 58386313 intron variant C/T snv 0.24 6
rs1047891
CPS1
0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 25
rs10479024 5 133131681 intergenic variant C/A;T snv 1
rs10483776
FUT8
14 65448149 intron variant A/G snv 0.13 1
rs10489615
GALNT2
1 230169242 intron variant A/C;G snv 2
rs10494363
OTUD7B ; MTMR11
1 149937602 upstream gene variant G/A snv 4.7E-02 1
rs10503669 0.925 0.080 8 19990179 intergenic variant C/A snv 8.4E-02 3
rs10504474
NCOA2
8 70348225 intron variant G/A snv 9.9E-02 1
rs10507274
C12orf49
1.000 0.040 12 116723171 missense variant T/C snv 4.7E-02 4.4E-02 2
rs1051921
MLXIPL
0.925 0.120 7 73593613 3 prime UTR variant G/A snv 0.15 2
rs1065853 19 44909976 non coding transcript exon variant G/A;C;T snv 4
rs10713774 4 26048829 intergenic variant C/- del 0.18 3
rs10743940
CD163
12 7498542 intron variant A/C;T snv 1
rs10744826
UBE3B
12 109527707 intron variant C/G snv 0.57 3
rs10761731
JMJD1C
10 63267850 intron variant A/T snv 0.38 6
rs10769254
MYBPC3
11 47340914 intron variant G/C snv 0.27 4
rs10773003
SBNO1
12 123290580 3 prime UTR variant G/A snv 0.11 1
rs10773105
SCARB1
12 124799220 intron variant C/T snv 0.63 1
rs10773112
SCARB1
12 124853983 intron variant C/T snv 0.63 1
rs1077834
LIPC ; ALDH1A2
15 58431280 intron variant T/C snv 0.34 4
rs1077835
ALDH1A2 ; LIPC
15 58431227 intron variant A/G snv 0.34 3
rs10789752
ZC3H12C ; RDX
11 110109220 intron variant T/A;C snv 1