Disease: High density lipoprotein measurement
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1011731
DNM3 ; PIGC
1 172377408 intron variant G/A snv 0.46 4
rs10127775
GALNT2
1 230160042 intron variant A/G;T snv 4
rs10864728
GALNT2
1 230169168 intron variant A/G snv 0.50 3
rs10900522
NUCKS1
1 205714939 3 prime UTR variant T/C snv 0.21 4
rs114165349
LOC101928728 ; ARID1A
1 26695422 intron variant G/C snv 1.7E-02 5
rs12748152 1.000 0.120 1 26811902 upstream gene variant C/T snv 5.7E-02 6
rs1321257
GALNT2
1 230169566 intron variant G/A snv 0.50 2
rs193084249 1 26661155 intergenic variant A/G snv 1.7E-02 3
rs2144300
GALNT2
0.882 0.040 1 230159169 intron variant C/T snv 0.44 2
rs2642438
MTARC1
1 220796686 missense variant A/G snv 0.75 0.78 6
rs2785990
LYPLAL1-AS1
1 219514090 intergenic variant C/T snv 0.73 2
rs2791547
LOC107985272 ; LYPLAL1-AS1
1 219486326 intergenic variant A/T snv 0.51 2
rs4495740
DOCK7
1 62658794 intron variant T/G snv 0.34 4
rs4846914
GALNT2
0.925 0.080 1 230159944 intron variant G/A snv 0.45 2
rs4846923
GALNT2
1 230171476 intron variant T/G snv 0.72 2
rs4847240
DR1
1 93352389 intron variant A/G snv 0.51 3
rs55878063
NFIA
1 61206237 intron variant G/A snv 0.12 2
rs629301
CELSR2
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 19
rs7519429
DNM3 ; PIGC
1 172380106 intron variant A/C snv 0.29 2
rs79598313
KDF1
1 26958422 intron variant C/A;T snv 5
rs1009360
LOC107984063 ; LINC02245 ; LINC02576
2 65048915 intron variant T/C snv 0.51 2
rs10184004 1.000 0.080 2 164651879 downstream gene variant C/T snv 0.48 5
rs10185855
TBC1D8
2 101025798 intron variant A/G snv 0.35 4
rs1041968
APOB
2 21009932 synonymous variant G/A snv 0.39 0.38 4
rs1042034
APOB
0.851 0.240 2 21002409 missense variant C/T snv 0.70 0.78 6