Disease: High density lipoprotein measurement
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1009360
LOC107984063 ; LINC02245 ; LINC02576
2 65048915 intron variant T/C snv 0.51 2
rs10096633 1.000 0.040 8 19973410 regulatory region variant C/T snv 0.22 2
rs10105606 8 19970337 downstream gene variant C/A snv 0.42 2
rs1145198 11 116703620 intergenic variant G/A snv 0.21 2
rs11765979
LOC105375508
7 130761118 intergenic variant A/C;G snv 2
rs11902417 2 20976028 intergenic variant G/A snv 0.25 2
rs11940232 4 137812732 intron variant C/T snv 0.22 2
rs11984636 8 20028215 intergenic variant T/C snv 8.3E-02 2
rs1321257
GALNT2
1 230169566 intron variant G/A snv 0.50 2
rs13240994
MLXIPL
7 73602532 intron variant T/C snv 0.16 2
rs13241165
LOC105375508
7 130747779 intergenic variant A/T snv 0.40 2
rs13263508
LOC105379311
8 20084670 intron variant G/T snv 0.58 2
rs133027
PLA2G6
22 38179492 intron variant T/- delins 0.46 2
rs13326165
STAB1
3 52498102 intron variant A/G;T snv 2
rs13702
LPL
0.925 0.160 8 19966981 3 prime UTR variant T/A;C snv 2
rs138570705
FRMD5
15 43974532 intron variant G/A snv 2.0E-02 2
rs139961185
SIK3
11 116936627 intron variant G/A snv 1.1E-02 2
rs142953140
PCSK7
11 117218489 missense variant C/T snv 1.9E-04 6.8E-04 2
rs148149124
TUBGCP4
15 43382233 intron variant TAAAAGAAAAA/-;TAAAAGAAAAATAAAAGAAAAA delins 2
rs149492745
TTBK2
15 42807352 intron variant C/T snv 1.7E-02 2
rs149580368 17 43797377 downstream gene variant C/A snv 2
rs150090666
PDE3B
11 14843853 stop gained C/G;T snv 8.0E-06; 5.8E-04 2
rs1515100 2 226264201 intergenic variant C/A snv 0.58 2
rs1519480
BDNF-AS
0.925 0.040 11 27654165 intron variant C/T snv 0.54 2
rs1562398
LOC105375508
7 130773172 intergenic variant C/G;T snv 2