Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1000879
VIL1
2 218439407 intron variant G/A snv 4.1E-02 3
rs10047459
APOA1-AS ; SIK3
11 116851110 intron variant C/T snv 0.80 1
rs10047462
APOA1-AS ; SIK3
11 116851325 intron variant G/C;T snv 2
rs10055011
CERT1
5 75502331 intron variant G/A snv 0.12 1
rs10096633 1.000 0.040 8 19973410 regulatory region variant C/T snv 0.22 7
rs10105606 8 19970337 downstream gene variant C/A snv 0.42 1
rs1011731
DNM3 ; PIGC
1 172377408 intron variant G/A snv 0.46 1
rs10118611
BNC2
9 16597467 intron variant G/A snv 3.0E-02 1
rs10119
TOMM40
0.925 0.080 19 44903416 3 prime UTR variant G/A snv 0.28 3
rs10120653
RXRA
9 134415237 intron variant G/T snv 1.2E-02 3
rs10125024
RXRA
9 134407131 intron variant C/T snv 1.5E-02 1
rs10138032
HIF1A ; HIF1A-AS3
14 61717464 intron variant A/G snv 8.8E-02 1
rs10156121 7 142672656 downstream gene variant T/C snv 3.9E-02 4
rs10195252
COBLL1
0.925 0.080 2 164656581 intron variant T/C snv 0.48 3
rs10198175 0.925 0.080 2 20934123 intergenic variant A/G snv 0.93 1
rs102275
TMEM258
0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 10
rs10305923
EDNRA
4 147539622 intron variant T/C snv 2.1E-02 1
rs1031045
LPL
8 19943601 intron variant G/A snv 0.12 3
rs1037814
AFF1
4 87128698 intron variant T/C snv 0.60 1
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 6
rs10402271 1.000 0.080 19 44825957 downstream gene variant T/G snv 0.28 6
rs10415849
GATAD2A
19 19394278 intron variant C/T snv 0.12 4
rs10419349
VAV1
19 6836678 intron variant C/T snv 2.5E-02 1
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 7