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: rs738409
rs738409
PNPLA3
88 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 0.800 1.000 29 2010 2019
dbSNP: rs2896019
rs2896019
PNPLA3
10 0.790 0.160 22 43937814 intron variant T/G snv 0.20 0.710 1.000 2 2013 2014
dbSNP: rs738491
rs738491
SAMM50 ; PNPLA3
3 0.882 0.040 22 43958231 intron variant C/T snv 0.34 0.710 1.000 2 2013 2015
dbSNP: rs1007863
rs1007863
SAMM50 ; PARVB
1 1.000 22 43999571 missense variant T/A;C snv 0.44 0.700 1.000 1 2013 2013
dbSNP: rs1010022
rs1010022
PNPLA3
1 1.000 22 43940430 intron variant A/G snv 0.20 0.700 1.000 1 2013 2013
dbSNP: rs1010023
rs1010023
PNPLA3
4 0.851 0.080 22 43940218 intron variant T/C snv 0.20 0.700 1.000 1 2013 2013
dbSNP: rs11090617
rs11090617
PNPLA3
1 1.000 22 43930820 intron variant C/T snv 0.18 0.700 1.000 1 2013 2013
dbSNP: rs12483959
rs12483959
PNPLA3
4 1.000 22 43930116 intron variant G/A;C;T snv 0.700 1.000 1 2013 2013
dbSNP: rs1461729
rs1461729
LOC157273
5 1.000 8 9329732 intron variant A/G snv 0.88 0.700 1.000 1 2013 2013
dbSNP: rs1474745
rs1474745
PNPLA3
1 1.000 22 43953356 intron variant T/C snv 0.19 0.700 1.000 1 2013 2013
dbSNP: rs1883349
rs1883349
PNPLA3
1 1.000 22 43936063 intron variant G/A snv 0.19 0.700 1.000 1 2013 2013
dbSNP: rs1883350
rs1883350
PNPLA3
1 1.000 22 43932163 intron variant T/C snv 0.35 0.700 1.000 1 2013 2013
dbSNP: rs1977081
rs1977081
PNPLA3
2 1.000 22 43934248 intron variant T/C;G snv 0.700 1.000 1 2013 2013
dbSNP: rs2072905
rs2072905
PNPLA3
1 1.000 22 43937599 intron variant C/G;T snv 0.700 1.000 1 2013 2013
dbSNP: rs2072907
rs2072907
PNPLA3
3 0.882 0.120 22 43936773 intron variant C/G snv 0.20 0.700 1.000 1 2013 2013
dbSNP: rs2073079
rs2073079
SAMM50
1 1.000 22 43989714 intron variant A/G snv 0.21 0.700 1.000 1 2013 2013
dbSNP: rs2073080
rs2073080
SAMM50 ; PARVB
2 0.925 0.040 22 43998522 intron variant C/T snv 0.20 0.700 1.000 1 2013 2013
dbSNP: rs2073081
rs2073081
PNPLA3
1 1.000 22 43939864 intron variant T/C snv 0.20 0.700 1.000 1 2013 2013
dbSNP: rs2076211
rs2076211
PNPLA3
3 1.000 22 43933198 intron variant C/A;T snv 0.18 0.700 1.000 1 2013 2013
dbSNP: rs2126259
rs2126259
LOC157273
9 1.000 8 9327636 intron variant T/C snv 0.87 0.700 1.000 1 2013 2013
dbSNP: rs2143571
rs2143571
SAMM50
5 0.827 0.080 22 43995806 intron variant G/A snv 0.25 0.700 1.000 1 2013 2013
dbSNP: rs2235776
rs2235776
SAMM50
3 0.925 0.040 22 43982119 intron variant C/T snv 0.24 0.700 1.000 1 2013 2013
dbSNP: rs2235777
rs2235777
SAMM50
1 1.000 22 43982929 intron variant C/T snv 0.24 0.700 1.000 1 2013 2013
dbSNP: rs2235778
rs2235778
SAMM50
1 1.000 22 43993634 intron variant T/C snv 0.48 0.700 1.000 1 2013 2013
dbSNP: rs2281135
rs2281135
PNPLA3
10 0.851 0.160 22 43936690 intron variant G/A snv 0.19 0.700 1.000 1 2013 2013