Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs4363657
rs4363657
SLCO1B1
5 12 21215788 intron variant T/C snv 0.18 0.020 1.000 2 2015 2019
dbSNP: rs1012657750
rs1012657750
SELENBP1
2 1 151368294 missense variant G/C snv 0.010 1.000 1 2020 2020
dbSNP: rs10488699
rs10488699
BUD13
1 11 116761784 intron variant C/T snv 1.0E-01 0.010 1.000 1 2017 2017
dbSNP: rs1121923
rs1121923
LPL
1 8 19951924 synonymous variant G/A snv 3.3E-02 5.6E-02 0.010 1.000 1 2019 2019
dbSNP: rs11542035
rs11542035
APOE
1 19 44908706 missense variant G/A snv 1.9E-05 2.8E-05 0.010 1.000 1 1995 1995
dbSNP: rs11961407
rs11961407
CCHCR1
2 6 31154630 missense variant G/A snv 3.0E-03 1.3E-02 0.010 1.000 1 2020 2020
dbSNP: rs12363280
rs12363280
SIRT3
1 11 231980 intron variant C/A;G snv 0.010 1.000 1 2015 2015
dbSNP: rs1249051329
rs1249051329
SELENBP1
2 1 151369834 synonymous variant T/C snv 3.5E-05 0.010 1.000 1 2020 2020
dbSNP: rs1263163
rs1263163 		2 11 116802796 intergenic variant G/A snv 0.10 0.010 1.000 1 2017 2017
dbSNP: rs1289389
rs1289389
SLC15A1
2 13 98684036 3 prime UTR variant C/T snv 0.18 0.010 1.000 1 2019 2019
dbSNP: rs1430583
rs1430583
UCP1
1 4 140565830 intron variant C/T snv 0.20 0.010 1.000 1 2015 2015
dbSNP: rs1685354
rs1685354
UCP3
1 11 74002546 intron variant A/G snv 0.30 0.010 1.000 1 2015 2015
dbSNP: rs1978124
rs1978124
ACE2
2 X 15599940 intron variant T/A;C snv 0.010 1.000 1 2018 2018
dbSNP: rs2070665
rs2070665
APOA1 ; APOA1-AS
2 11 116836968 intron variant A/C;G snv 0.85 0.010 < 0.001 1 2016 2016
dbSNP: rs2075294
rs2075294
ZPR1
1 11 116787406 intron variant G/T snv 3.5E-02 0.010 1.000 1 2019 2019
dbSNP: rs217428
rs217428
NPC1L1
1 7 44515974 intron variant T/G snv 0.21 0.26 0.010 1.000 1 2014 2014
dbSNP: rs217434
rs217434
NPC1L1
1 7 44513639 synonymous variant A/G snv 0.16 0.17 0.010 1.000 1 2014 2014
dbSNP: rs2187126
rs2187126
BUD13
2 11 116765068 intron variant A/G snv 4.8E-02 0.010 1.000 1 2017 2017
dbSNP: rs2229268
rs2229268
LRP2
1 2 169168573 synonymous variant A/G snv 0.20 0.16 0.010 1.000 1 2014 2014
dbSNP: rs233575
rs233575
ACE2
1 X 15564843 intron variant G/A snv 0.010 1.000 1 2018 2018
dbSNP: rs258
rs258
LPL
4 8 19954741 intron variant G/A;C;T snv 0.010 1.000 1 2019 2019
dbSNP: rs3060
rs3060
DGAT2
1 11 75800527 3 prime UTR variant T/C snv 0.14 0.22 0.010 1.000 1 2015 2015
dbSNP: rs4646142
rs4646142
ACE2
1 X 15584941 intron variant G/A;C snv 0.010 1.000 1 2018 2018
dbSNP: rs4646156
rs4646156
ACE2
2 X 15578920 intron variant A/T snv 0.010 1.000 1 2018 2018
dbSNP: rs5072
rs5072
APOA1 ; APOA1-AS
5 11 116836867 intron variant A/G snv 0.89 0.010 1.000 1 2019 2019