Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1815739
ACTN3
0.763 0.240 11 66560624 stop gained C/T snv 0.37 1
rs16940170
ALDH1A2
1.000 0.040 15 58392083 intron variant G/A snv 0.15 1
rs495348
ALDH1A2
1.000 0.040 15 58395591 intron variant C/G snv 0.82 1
rs11631342
ALDH1A2 ; LIPC
1.000 0.040 15 58432184 non coding transcript exon variant A/G snv 5.6E-02 1
rs670
APOA1 ; APOA1-AS
0.763 0.360 11 116837697 5 prime UTR variant C/T snv 0.17 1
rs5128
APOC3
0.925 0.080 11 116832924 3 prime UTR variant G/C snv 0.84 0.87 1
rs405509
APOE
0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58 1
rs769450
APOE
0.925 0.120 19 44907187 non coding transcript exon variant G/A snv 0.39 1
rs11820589
BUD13
1.000 0.040 11 116763146 missense variant G/A snv 7.8E-02 0.10 1
rs1127065
CAMK2B
1.000 0.040 7 44220272 synonymous variant C/G;T snv 1.7E-02; 0.41 1
rs11065756
CCDC63
0.925 0.080 12 110900990 intron variant C/T snv 6.1E-02 1
rs11063069
CCND2-AS1
0.925 0.080 12 4265207 intron variant A/G snv 0.20 1
rs3211931
CD36
0.925 0.080 7 80668857 intron variant C/T snv 0.38 1
rs12051272
CDH13
0.925 0.120 16 82629683 intron variant G/C;T snv 1
rs9465871
CDKAL1
0.882 0.120 6 20717024 intron variant T/C snv 0.30 1
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40 1
rs2383207
CDKN2B-AS1
0.695 0.280 9 22115960 intron variant A/G snv 0.64 1
rs16944558
COLEC12
1.000 0.040 18 442441 intron variant C/T snv 0.16 1
rs3091244
CRP
0.724 0.280 1 159714875 upstream gene variant G/A;T snv 1
rs225014
DIO2
0.695 0.400 14 80203237 missense variant T/C snv 0.41 0.39 1
rs8060686
EDC4
1.000 0.040 16 67877614 synonymous variant T/C snv 0.23 0.32 1
rs2241883
FABP1
0.763 0.360 2 88124547 missense variant T/C snv 0.30 0.29 1
rs7202116
FTO
0.882 0.120 16 53787703 intron variant A/G snv 0.41 1
rs4846922
GALNT2
1.000 0.040 1 230171436 intron variant T/A;C;G snv 1
rs2293571
GCKR
0.882 0.120 2 27506613 non coding transcript exon variant G/A snv 0.40 0.39 1