Disease: High density lipoprotein measurement
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 34
rs13114738
SLC39A8
0.851 0.120 4 102363708 intron variant C/A;T snv 16
rs629301
CELSR2
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 22
rs6533530 0.851 0.120 4 110810780 intergenic variant T/C snv 0.47 16
rs12229654 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 20
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs11065987 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 17
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 22
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs7115242
SIK3
0.851 0.120 11 117037567 intron variant A/G;T snv 16
rs2257129
LOC105378522
1.000 0.040 10 121139183 regulatory region variant T/C snv 0.82 3
rs12369179
ZCCHC8
0.851 0.120 12 122479003 intron variant C/T snv 5.9E-02 16
rs12420422 0.851 0.120 11 123009573 intergenic variant G/A snv 3.4E-02 16
rs7632505
SEMA5B
0.827 0.120 3 123019460 intron variant A/G snv 0.34 17
rs2980853 0.851 0.120 8 125466108 upstream gene variant A/C snv 0.43 16
rs2954021 1.000 0.040 8 125469835 intron variant A/G snv 0.54 15
rs7621025
STAG1
3 136553404 intron variant T/A;C snv 3
rs1869717
MAML3
0.851 0.120 4 139829967 intron variant G/C snv 0.14 16
rs11727676
HHIP
0.776 0.080 4 144737912 synonymous variant T/C snv 6.6E-02 6.4E-02 14
rs222826 0.851 0.120 2 146120964 regulatory region variant T/C snv 0.94 16
rs4691380
PDGFC
4 156798972 intron variant C/T snv 0.45 4
rs12328675
COBLL1
2 164684290 3 prime UTR variant T/C snv 0.13 4
rs7607980
COBLL1
1.000 0.080 2 164694691 missense variant T/C snv 0.11 0.13 8
rs7730898
RANBP17
5 171032671 intron variant G/A snv 0.75 2
rs9816226
DGKG
1.000 0.080 3 186116710 intron variant A/T snv 0.82 5