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: 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 2014 2014
dbSNP: rs1229984
rs1229984
ADH1B
83 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 0.700 1.000 4 2013 2019
dbSNP: rs1260326
rs1260326
GCKR
81 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 0.700 1.000 1 2019 2019
dbSNP: rs1421085
rs1421085
FTO
28 0.752 0.280 16 53767042 intron variant T/C snv 0.31 0.700 1.000 1 2019 2019
dbSNP: rs11066001
rs11066001
BRAP
15 0.763 0.360 12 111681367 intron variant T/C snv 5.8E-03 0.700 1.000 1 2019 2019
dbSNP: rs13107325
rs13107325
SLC39A8
34 0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 0.700 1.000 1 2019 2019
dbSNP: rs2066702
rs2066702
ADH1B
7 0.882 0.080 4 99307860 missense variant G/A snv 1.5E-02 5.9E-02 0.700 1.000 2 2014 2019
dbSNP: rs10392
rs10392
PPP1R16B
6 0.882 0.160 20 38922292 3 prime UTR variant G/A snv 0.17 0.700 1.000 1 2017 2017
dbSNP: rs139438618
rs139438618
SEMA3A
5 0.882 0.080 7 84008281 intron variant A/G snv 5.2E-02 0.700 1.000 1 2017 2017
dbSNP: rs10196867
rs10196867
CTNNA2
5 0.925 0.080 2 79751234 intron variant C/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs10198241
rs10198241 		4 0.925 0.080 2 226115660 intergenic variant T/C snv 0.58 0.700 1.000 1 2017 2017
dbSNP: rs115357105
rs115357105 		4 0.925 0.080 9 104376689 intergenic variant A/G snv 1.5E-02 0.700 1.000 1 2017 2017
dbSNP: rs11825659
rs11825659
IGSF9B
4 0.925 0.080 11 133925624 intron variant A/G snv 0.12 0.700 1.000 1 2017 2017
dbSNP: rs12180309
rs12180309 		4 0.925 0.080 6 91209048 intergenic variant C/T snv 1.9E-02 0.700 1.000 1 2017 2017
dbSNP: rs12544026
rs12544026
NCALD
4 0.925 0.080 8 101819970 intron variant G/A snv 0.85 0.700 1.000 1 2017 2017
dbSNP: rs147247472
rs147247472
AGBL4 ; AGBL4-IT1
5 0.925 0.080 1 49441901 intron variant G/A snv 7.3E-04 0.700 1.000 1 2019 2019
dbSNP: rs1614972
rs1614972
ADH1B ; ADH1C
4 0.925 0.160 4 99336998 intron variant C/T snv 0.38 0.700 1.000 1 2014 2014
dbSNP: rs1789924
rs1789924
ADH1C
5 0.925 0.160 4 99353129 upstream gene variant C/G;T snv 0.700 1.000 1 2017 2017
dbSNP: rs2094081
rs2094081
RHBDL2
4 0.925 0.080 1 38927359 intron variant G/A;C snv 0.700 1.000 1 2017 2017
dbSNP: rs2133896
rs2133896
ANKS1B
5 0.925 0.080 12 99455122 intron variant G/T snv 7.6E-02 0.700 1.000 1 2019 2019
dbSNP: rs55702914
rs55702914 		4 0.925 0.080 2 197349672 intergenic variant C/G snv 0.37 0.700 1.000 1 2017 2017
dbSNP: rs58598658
rs58598658
KLF12
4 0.925 0.080 13 73887725 intron variant -/A;AA delins 0.700 1.000 1 2017 2017
dbSNP: rs72737330
rs72737330
ESRRG
4 0.925 0.080 1 216600151 intron variant T/C snv 0.15 0.700 1.000 1 2017 2017
dbSNP: rs79246196
rs79246196
STAG3
4 0.925 0.080 7 100185286 intron variant C/T snv 1.8E-02 0.700 1.000 1 2017 2017
dbSNP: rs1000579
rs1000579
STX18-AS1
3 1.000 0.080 4 4717767 intron variant A/G snv 0.44 0.700 1.000 2 2012 2017