Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs233575
ACE2
X 15564843 intron variant G/A snv 1
rs4646142
ACE2
X 15584941 intron variant G/A;C snv 1
rs11542035
APOE
19 44908706 missense variant G/A snv 1.9E-05 2.8E-05 1
rs10488699
BUD13
11 116761784 intron variant C/T snv 1.0E-01 1
rs7003945
DGAT1
8 144326802 5 prime UTR variant G/A;C snv 1
rs3060
DGAT2
11 75800527 3 prime UTR variant T/C snv 0.14 0.22 1
rs66698963
FADS2
11 61835025 intron variant ACTTCTCCCTGCCTCCCCAGGGACTTCTCCCTGCCTCCCCAGGG/-;ACTTCTCCCTGCCTCCCCAGGG delins 0.56 1
rs770730728
GCK ; LOC105375258
7 44147757 synonymous variant G/A snv 4.0E-06 7.0E-06 1
rs730882087
LDLR
19 11106640 missense variant GG/AC mnv 1
rs1121923
LPL
8 19951924 synonymous variant G/A snv 3.3E-02 5.6E-02 1
rs2229268
LRP2
2 169168573 synonymous variant A/G snv 0.20 0.16 1
rs217428
NPC1L1
7 44515974 intron variant T/G snv 0.21 0.26 1
rs217434
NPC1L1
7 44513639 synonymous variant A/G snv 0.16 0.17 1
rs751671151
PLAT
8 42180286 missense variant A/G snv 4.0E-06 1.4E-05 1
rs12363280
SIRT3
11 231980 intron variant C/A;G snv 1
rs1430583
UCP1
4 140565830 intron variant C/T snv 0.20 1
rs1685354
UCP3
11 74002546 intron variant A/G snv 0.30 1
rs2075294
ZPR1
11 116787406 intron variant G/T snv 3.5E-02 1
rs11774572 1.000 0.040 8 11589291 regulatory region variant C/G;T snv 2
rs1263163 11 116802796 intergenic variant G/A snv 0.10 2
rs4149339
ABCA1
1.000 0.040 9 104782875 3 prime UTR variant G/A snv 0.32 2
rs4743763
ABCA1
1.000 0.040 9 104830901 intron variant A/C;T snv 0.36 2
rs1978124
ACE2
X 15599940 intron variant T/A;C snv 2
rs4646156
ACE2
X 15578920 intron variant A/T snv 2
rs5069
APOA1-AS ; APOA1
1.000 0.080 11 116837538 5 prime UTR variant G/A snv 0.11 2