Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2001945 8 125465736 upstream gene variant G/A;C;T snv 6
rs2965101 1.000 0.080 19 44734556 intergenic variant T/C snv 0.34 6
rs2980869 8 125476008 intron variant C/T snv 0.48 6
rs2980875 8 125469505 intron variant A/C;G;T snv 6
rs2980880 8 125468730 intron variant G/A snv 0.69 6
rs515135 0.807 0.160 2 21063185 intergenic variant T/C snv 0.73 6
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 6
rs583104 1 109278685 downstream gene variant G/T snv 0.63 6
rs6982636 8 125467073 intron variant G/A snv 0.43 6
rs9622186 22 35377961 upstream gene variant A/G snv 3.7E-03 6
rs35381288
ADRB3
8 37965106 non coding transcript exon variant C/G snv 7.4E-03 6
rs34183407
ALMS1
2 73454052 missense variant C/T snv 2.1E-05 3.5E-05 6
rs533617
APOB
2 21011100 missense variant T/C snv 3.1E-02 2.9E-02 6
rs737410
ARRB1
11 75315038 intron variant A/G snv 4.3E-02 6
rs4803750
BCL3
0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 6
rs4970834
CELSR2
0.925 0.160 1 109272258 intron variant C/T snv 0.17 0.21 6
rs33980385
CYP2B6
19 40991388 missense variant A/G snv 6
rs760242
DHCR7
11 71435530 missense variant C/T snv 2.2E-04 6.3E-05 6
rs11570255
EDN3
1.000 20 59300861 missense variant G/A;T snv 3.3E-03; 2.9E-05 6
rs9341023
ESR1
6 152062578 intron variant C/T snv 6
rs3093267
F7
13 113118661 missense variant G/A;T snv 8.0E-05 6
rs1169288
HNF1A-AS1 ; HNF1A
0.776 0.160 12 120978847 missense variant A/C;T snv 0.35 6
rs4251583
IRAK4
12 43783705 missense variant A/G snv 8.6E-04 1.1E-03 6
rs2230667
IRF3
19 49662445 missense variant C/T snv 1.0E-04 1.4E-05 6
rs17240378
LCAT
16 67942790 intron variant G/C;T snv 4.0E-06 6