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: rs12373751
rs12373751
ERBB4
1 1.000 0.040 2 212072166 intron variant T/C snv 0.62 0.700 1.000 1 2019 2019
dbSNP: rs139271658
rs139271658
PTPRD
2 1.000 0.040 9 9797383 intron variant A/G snv 1.9E-02 0.700 1.000 1 2019 2019
dbSNP: rs1881396
rs1881396
ZNF512
1 1.000 0.040 2 27621734 3 prime UTR variant T/A;G snv 0.700 1.000 1 2018 2018
dbSNP: rs1953124
rs1953124 		1 1.000 0.040 13 65771915 regulatory region variant C/A;G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs206833
rs206833 		3 1.000 0.040 2 31485750 intergenic variant G/A snv 0.17 0.700 1.000 1 2019 2019
dbSNP: rs2235776
rs2235776
SAMM50
3 0.925 0.040 22 43982119 intron variant C/T snv 0.24 0.700 1.000 1 2012 2012
dbSNP: rs2294915
rs2294915
PNPLA3
5 1.000 0.040 22 43945024 intron variant C/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs2668423
rs2668423
PWWP3A
1 1.000 0.040 19 1370527 intron variant T/G snv 0.73 0.700 1.000 1 2018 2018
dbSNP: rs2710833
rs2710833
DDX60L ; LOC107986198
2 0.925 0.080 4 168488807 intron variant T/A;C snv 0.700 1.000 1 2010 2010
dbSNP: rs2980888
rs2980888 		2 1.000 0.040 8 125495066 intron variant T/C snv 0.76 0.700 1.000 1 2019 2019
dbSNP: rs4808199
rs4808199
GATAD2A ; MIR640
5 1.000 0.040 19 19434290 intron variant G/A;T snv 0.19 0.700 1.000 1 2018 2018
dbSNP: rs497408
rs497408 		1 1.000 0.040 6 23993395 regulatory region variant C/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs6006611
rs6006611
SAMM50 ; PARVB
1 1.000 0.040 22 44004818 intron variant G/A snv 0.44 0.700 1.000 1 2013 2013
dbSNP: rs6128907
rs6128907
ACTR5
1 1.000 0.040 20 38759219 intron variant T/C snv 0.17 0.700 1.000 1 2017 2017
dbSNP: rs62141163
rs62141163 		2 1.000 0.040 2 31440248 regulatory region variant G/A snv 7.6E-02 0.700 1.000 1 2019 2019
dbSNP: rs6487679
rs6487679 		2 0.925 0.080 12 9218736 intergenic variant C/T snv 0.80 0.700 1.000 1 2010 2010
dbSNP: rs6499186
rs6499186 		1 1.000 0.040 16 68626662 downstream gene variant C/T snv 0.84 0.700 1.000 1 2019 2019
dbSNP: rs6591182
rs6591182
EHBP1L1
2 0.925 0.080 11 65582285 missense variant T/G snv 0.47 0.45 0.700 1.000 1 2010 2010
dbSNP: rs71413689
rs71413689 		1 1.000 0.040 2 150398953 intergenic variant G/A snv 1.7E-02 0.700 1.000 1 2019 2019
dbSNP: rs72943235
rs72943235 		1 1.000 0.040 2 88201127 intergenic variant G/A snv 9.0E-02 0.700 1.000 1 2019 2019
dbSNP: rs887304
rs887304
CRACR2A
2 0.925 0.080 12 3648382 3 prime UTR variant T/C snv 0.77 0.700 1.000 1 2010 2010
dbSNP: rs9817981
rs9817981
TP63
1 1.000 0.040 3 189845741 intron variant A/G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs58542926
rs58542926
TM6SF2
42 0.630 0.440 19 19268740 missense variant C/T snv 6.5E-02 5.8E-02 0.100 0.905 42 2014 2020
dbSNP: rs641738
rs641738
MBOAT7 ; TMC4 ; LOC112268246
22 0.689 0.320 19 54173068 missense variant T/A;C;G snv 0.100 0.917 12 2016 2019
dbSNP: rs1801282
rs1801282
PPARG
131 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.090 0.778 9 2010 2014