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: rs1229984
rs1229984
ADH1B
83 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 0.700 1.000 1 2019 2019
dbSNP: rs12581220
rs12581220 		1 12 78379471 intron variant C/T snv 0.28 0.700 1.000 1 2019 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: rs13163314
rs13163314 		1 5 148710024 intergenic variant C/T snv 0.18 0.700 1.000 1 2019 2019
dbSNP: rs141086701
rs141086701
TSNARE1
1 8 142280097 stop gained G/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs1437971
rs1437971 		1 2 100370502 non coding transcript exon variant A/C snv 0.78 0.75 0.700 1.000 1 2019 2019
dbSNP: rs148173957
rs148173957
LOC105378976
2 1.000 0.040 5 56078195 intron variant TT/- del 8.2E-02 0.700 1.000 1 2019 2019
dbSNP: rs1513481
rs1513481
ARPP21
1 3 35742043 intron variant C/T snv 0.27 0.700 1.000 1 2019 2019
dbSNP: rs1516187
rs1516187
LOC730100
1 2 51703026 intron variant T/C snv 0.89 0.700 1.000 1 2019 2019
dbSNP: rs1562308
rs1562308 		1 2 61541286 upstream gene variant A/C;T snv 0.700 1.000 1 2019 2019
dbSNP: rs16850592
rs16850592 		1 2 165408506 regulatory region variant T/C snv 0.21 0.700 1.000 1 2019 2019
dbSNP: rs17123039
rs17123039
PYGL
1 14 50865617 non coding transcript exon variant T/G snv 0.35 0.700 1.000 1 2019 2019
dbSNP: rs17635778
rs17635778 		1 9 119402824 intergenic variant C/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs1957111
rs1957111
LOC102724934
1 14 29311972 intron variant C/T snv 4.1E-02 0.700 1.000 1 2019 2019
dbSNP: rs1996928
rs1996928
LINC01524 ; LOC105372666
1 20 52644875 intron variant G/A snv 0.27 0.700 1.000 1 2019 2019
dbSNP: rs2393831
rs2393831
CABCOCO1
1 10 61706996 intron variant A/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs2422137
rs2422137
NEGR1
1 1 72154278 intron variant C/A snv 0.37 0.700 1.000 1 2019 2019
dbSNP: rs2472297
rs2472297 		9 0.882 0.160 15 74735539 intergenic variant C/T snv 0.16 0.700 1.000 1 2019 2019
dbSNP: rs2504671
rs2504671 		1 6 51340779 intergenic variant C/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs2761589
rs2761589
DCDC1
1 11 31289882 intron variant C/A;G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs2945091
rs2945091
LINC02742
1 11 28824022 intron variant G/A snv 0.45 0.700 1.000 1 2019 2019
dbSNP: rs2968426
rs2968426
GSE1 ; LOC107984830
1 16 85302129 intron variant G/C;T snv 0.700 1.000 1 2019 2019
dbSNP: rs33951980
rs33951980
MLXIPL
3 7 73615107 intron variant C/T snv 0.10 0.700 1.000 1 2019 2019
dbSNP: rs34452566
rs34452566 		1 11 27771923 intron variant G/T snv 0.14 0.700 1.000 1 2019 2019
dbSNP: rs34783010
rs34783010
GIPR
1 19 45677156 intron variant G/T snv 0.18 0.17 0.700 1.000 1 2019 2019