Source: INFERRED ×
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 10
rs2126259
LOC157273
1.000 8 9327636 intron variant T/C snv 0.87 9
rs630014
ABO
9 133274306 intron variant G/A;C snv 9
rs12721046
APOC1
19 44917997 intron variant G/A snv 0.11 8
rs11570255
EDN3
1.000 20 59300861 missense variant G/A;T snv 3.3E-03; 2.9E-05 7
rs11902417 2 20976028 intergenic variant G/A snv 0.25 7
rs6982636 8 125467073 intron variant G/A snv 0.43 7
rs8177318
INHCAP ; TF
3 133748533 missense variant T/A snv 1.6E-04 2.9E-04 7
rs1041968
APOB
2 21009932 synonymous variant G/A snv 0.39 0.38 6
rs11568746
TGFBR1
9 99105926 intron variant C/G snv 2.1E-05 6
rs11571151
PGR-AS1 ; PGR
11 101127486 missense variant C/G;T snv 6
rs1167998
DOCK7
1 62465961 intron variant C/A snv 0.57 6
rs17240378
LCAT
16 67942790 intron variant G/C;T snv 4.0E-06 6
rs1801689
APOH
17 66214462 missense variant A/C;G snv 4.0E-06; 2.4E-02; 4.8E-05 6
rs1874148
VCL
10 74114657 intron variant A/G snv 1.8E-02 6
rs2230667
IRF3
19 49662445 missense variant C/T snv 1.0E-04 1.4E-05 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
rs3093267
F7
13 113118661 missense variant G/A;T snv 8.0E-05 6
rs33980385
CYP2B6
19 40991388 missense variant A/G snv 6
rs34090729
RXRA
9 134401999 non coding transcript exon variant C/T snv 1.6E-04 3.6E-04 6
rs34183407
ALMS1
2 73454052 missense variant C/T snv 2.1E-05 3.5E-05 6
rs35381288
ADRB3
8 37965106 non coding transcript exon variant C/G snv 7.4E-03 6
rs35980686
MIR8085 ; BCL3
19 44757093 missense variant T/C snv 1.1E-03 4.4E-03 6