Source: CURATED ×
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: rs9791817
rs9791817
GRB10
1 1.000 0.120 7 50593490 intron variant C/G snv 0.45 0.700 1.000 1 2013 2013
dbSNP: rs936094
rs936094
RXFP1
1 1.000 0.120 4 158523162 intron variant T/A;C;G snv 0.700 1.000 1 2012 2012
dbSNP: rs924607
rs924607
LOC100996325 ; LOC105374608
3 0.851 0.120 5 609978 intron variant C/T snv 0.32 0.700 1.000 1 2015 2015
dbSNP: rs920590
rs920590 		3 1.000 0.120 8 19793650 regulatory region variant T/C snv 0.39 0.700 1.000 1 2012 2012
dbSNP: rs8015478
rs8015478
CEBPE
2 1.000 0.120 14 23116809 downstream gene variant A/C snv 0.68 0.700 1.000 1 2013 2013
dbSNP: rs7923074
rs7923074
ARID5B
1 1.000 0.120 10 61963681 intron variant A/C snv 0.56 0.700 1.000 1 2013 2013
dbSNP: rs79050301
rs79050301
TPMT
1 1.000 0.120 6 18151959 intron variant T/C snv 4.5E-02 0.700 1.000 1 2018 2018
dbSNP: rs7901152
rs7901152
PIP4K2A
1 1.000 0.120 10 22544224 intron variant G/A snv 0.66 0.700 1.000 1 2013 2013
dbSNP: rs7896246
rs7896246
ARID5B
1 0.925 0.120 10 61964631 intron variant A/G snv 0.74 0.710 1.000 1 2013 2017
dbSNP: rs7818688
rs7818688
NDUFAF6
3 1.000 0.120 8 95011854 intron variant C/A;G snv 0.700 1.000 1 2015 2015
dbSNP: rs780963440
rs780963440
SETD2
1 1.000 0.120 3 47123960 missense variant G/A;C snv 5.0E-05; 1.3E-05 0.700 1.000 2 2014 2014
dbSNP: rs7808025
rs7808025
DDC ; FIGNL1
1 1.000 0.120 7 50509205 intron variant G/A;C snv 0.28 0.700 1.000 1 2013 2013
dbSNP: rs7806674
rs7806674
IKZF1
1 1.000 0.120 7 50356265 intron variant C/A;G snv 0.700 1.000 1 2013 2013
dbSNP: rs7803247
rs7803247
DDC ; FIGNL1
1 1.000 0.120 7 50473045 intron variant T/C snv 0.52 0.700 1.000 1 2013 2013
dbSNP: rs7791875
rs7791875
DDC ; FIGNL1
1 1.000 0.120 7 50503190 intron variant C/T snv 1.0E-01 0.700 1.000 1 2013 2013
dbSNP: rs74709575
rs74709575
LINC02334
3 1.000 0.120 13 38041119 intron variant A/C snv 3.1E-03 0.700 1.000 1 2017 2017
dbSNP: rs738409
rs738409
PNPLA3
13 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 0.700 1.000 1 2017 2017
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 2017 2017
dbSNP: rs73195662
rs73195662
CDHR3
1 1.000 0.120 7 106018014 missense variant C/A;G;T snv 7.2E-02; 2.0E-05 0.700 1.000 1 2019 2019
dbSNP: rs73062673
rs73062673
CNOT3 ; LOC102724273
1 1.000 0.120 19 54151243 intron variant T/C snv 1.0E-01 0.700 1.000 1 2019 2019
dbSNP: rs72772090
rs72772090
CAST
3 1.000 0.120 5 96700607 intron variant G/A;C snv 0.700 1.000 1 2017 2017
dbSNP: rs7156960
rs7156960
GPATCH2L ; LOC105370575
1 1.000 0.120 14 76237008 intron variant C/G;T snv 0.800 1.000 1 2012 2012
dbSNP: rs7142143
rs7142143
PYGL
1 1.000 0.120 14 50936813 intron variant T/C snv 2.8E-02 0.800 1.000 1 2012 2012
dbSNP: rs7089424
rs7089424
ARID5B
3 0.752 0.200 10 61992400 intron variant T/G snv 0.32 0.800 1.000 2 2009 2018
dbSNP: rs7088318
rs7088318
PIP4K2A
1 0.851 0.120 10 22564019 intron variant C/A snv 0.55 0.700 1.000 1 2013 2013