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: rs2896019
rs2896019
PNPLA3
10 0.790 0.160 22 43937814 intron variant T/G snv 0.20 0.700 1.000 1 2010 2010
dbSNP: rs3747207
rs3747207
PNPLA3
7 22 43928975 intron variant G/A snv 0.22 0.700 1.000 1 2019 2019
dbSNP: rs4823173
rs4823173
PNPLA3
8 0.827 0.200 22 43932850 intron variant G/A snv 0.24 0.18 0.700 1.000 1 2019 2019
dbSNP: rs738408
rs738408
PNPLA3
10 0.925 0.120 22 43928850 synonymous variant C/T snv 0.28 0.22 0.700 1.000 1 2018 2018
dbSNP: rs11878604
rs11878604 		5 19 40827379 intron variant T/C snv 0.14 0.700 1.000 1 2018 2018
dbSNP: rs34010237
rs34010237
FCGRT
3 19 49509317 intron variant G/A snv 0.13 0.700 1.000 1 2018 2018
dbSNP: rs138424361
rs138424361 		1 18 61567782 downstream gene variant G/A snv 9.3E-03 0.700 1.000 1 2019 2019
dbSNP: rs73550818
rs73550818
GOT2
1 16 58730951 intron variant C/A snv 0.12 0.700 1.000 1 2018 2018
dbSNP: rs862946
rs862946
LINC02306
1 14 26019261 intron variant T/C snv 0.77 0.700 1.000 1 2013 2013
dbSNP: rs11066280
rs11066280
HECTD4
27 0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 0.700 1.000 1 2019 2019
dbSNP: rs11067592
rs11067592 		2 12 109631385 intergenic variant G/T snv 1.2E-03 0.700 1.000 1 2018 2018
dbSNP: rs12231737
rs12231737
TRAFD1
5 0.925 0.120 12 112136812 intron variant C/T snv 5.9E-03 0.700 1.000 1 2019 2019
dbSNP: rs12580745
rs12580745
TMEM132D
1 12 129167622 intron variant T/C snv 3.5E-02 0.700 1.000 1 2019 2019
dbSNP: rs671
rs671
ALDH2
116 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 0.700 1.000 1 2019 2019
dbSNP: rs686288
rs686288
ANO4
1 12 100982873 intron variant A/G snv 4.6E-02 0.700 1.000 1 2019 2019
dbSNP: rs79105258
rs79105258
CUX2
24 12 111280427 intron variant C/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs11820744
rs11820744
OSBPL5 ; LOC107987158
2 1.000 0.040 11 3147308 intron variant C/T snv 0.23 0.700 1.000 1 2019 2019
dbSNP: rs12803802
rs12803802
SLC35F2
1 11 107800953 intron variant A/G snv 0.14 0.700 1.000 1 2019 2019
dbSNP: rs17342773
rs17342773
ABTB2
1 11 34322165 intron variant C/T snv 1.8E-02 0.700 1.000 1 2019 2019
dbSNP: rs74913549
rs74913549
PANX1
3 11 94180526 intron variant T/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs76850691
rs76850691
GOT1
1 10 99397681 stop gained G/A;C snv 4.0E-06; 5.2E-03 0.700 1.000 2 2013 2019
dbSNP: rs10509735
rs10509735
CNNM1
1 10 99372525 intron variant A/C snv 0.56 0.700 1.000 1 2018 2018
dbSNP: rs10827785
rs10827785 		1 10 17933413 intergenic variant T/C snv 0.25 0.700 1.000 1 2018 2018
dbSNP: rs118107800
rs118107800
PDCD4 ; PDCD4-AS1
1 10 110871498 non coding transcript exon variant T/C snv 2.0E-02 0.700 1.000 1 2019 2019
dbSNP: rs144430312
rs144430312
STAM
1 10 17693720 intron variant T/C snv 3.4E-04 0.700 1.000 1 2018 2018