Disease: response to simvastatin
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10034465
LINC02484
1.000 0.080 4 34193882 intron variant G/A snv 9.1E-02 2
rs112209655
LOC102724680
1.000 0.080 12 84947358 intergenic variant C/T snv 1.0E-02 2
rs112284299
PEX5L
1.000 0.080 3 179850308 intron variant G/C snv 1.6E-02 2
rs113816795 1.000 0.080 5 99159794 intergenic variant T/C snv 8.1E-03 2
rs114007472 1.000 0.080 8 63563681 intergenic variant G/A snv 9.4E-03 2
rs115092681
NLGN1
1.000 0.080 3 174201323 intron variant G/A;C;T snv 2
rs115990514
LOC107986066
1.000 0.080 3 19055898 intergenic variant C/A snv 9.0E-03 2
rs116616455 1.000 0.080 12 58041829 intergenic variant T/C snv 1.4E-02 2
rs117168171 1.000 0.080 15 101854599 downstream gene variant C/G;T snv 2
rs138270994 1.000 0.080 13 22791997 intergenic variant TCTTTG/- delins 2.3E-02 2
rs141864436
NRXN1
1.000 0.080 2 50971652 intron variant G/A snv 1.6E-02 2
rs143838781
RBM19
1.000 0.080 12 113940539 intron variant G/A snv 7.0E-03 2
rs145010525
DARS1
1.000 0.080 2 135975206 intron variant G/A snv 7.8E-03 2
rs146807753 1.000 0.080 6 3904005 downstream gene variant C/A;T snv 2
rs181126208
EDARADD
1.000 0.080 1 236495210 intron variant G/A snv 4.9E-02 2
rs250567 1.000 0.080 16 23383078 downstream gene variant C/T snv 8.1E-02 2
rs2607653
FGF14
1.000 0.080 13 102066314 intron variant A/G snv 5.9E-02 2
rs2631781
ST6GALNAC3
1.000 0.080 1 76128101 intron variant C/A;T snv 2
rs2823310 1.000 0.080 21 15497529 intron variant C/A snv 4.0E-02 2
rs34030778
CLN8
1.000 0.080 8 1771328 missense variant C/T snv 2.8E-03 1.1E-02 2
rs4988198
MCM6
1.000 0.080 2 135861240 intron variant T/C;G snv 2
rs57504626
PBX4
1.000 0.080 19 19609590 intron variant C/T snv 0.10 2
rs58847779
TRIOBP
1.000 0.080 22 37736644 intron variant T/C snv 4.4E-02 2
rs62210650 1.000 0.080 21 19649854 intergenic variant C/T snv 8.0E-02 2
rs6693796
PRRX1
1.000 0.080 1 170674137 intron variant T/C snv 7.7E-02 2