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: rs10136360
rs10136360
NRXN3
1 14 79427703 intron variant G/A snv 0.21 0.700 1.000 1 2019 2019
dbSNP: rs1036336
rs1036336
PLCL1
1 2 198099396 intron variant T/C snv 0.45 0.700 1.000 1 2019 2019
dbSNP: rs10457480
rs10457480 		1 6 126491463 intron variant C/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs11104632
rs11104632 		2 12 87829908 intergenic variant G/A snv 0.16 0.700 1.000 1 2016 2016
dbSNP: rs11109811
rs11109811 		1 12 78448289 intron variant C/G snv 0.12 0.700 1.000 1 2018 2018
dbSNP: rs113918189
rs113918189
CEP83
2 12 94325241 intron variant C/T snv 6.9E-02 0.700 1.000 1 2018 2018
dbSNP: rs11584700
rs11584700
LOC105371692
1 1 204607855 intron variant A/G snv 0.17 0.700 1.000 1 2019 2019
dbSNP: rs11642015
rs11642015
FTO
9 0.925 0.120 16 53768582 intron variant C/T snv 0.31 0.700 1.000 1 2019 2019
dbSNP: rs11646118
rs11646118
KCTD13 ; ASPHD1
1 16 29915150 non coding transcript exon variant T/C snv 5.6E-02 0.700 1.000 1 2019 2019
dbSNP: rs117287096
rs117287096 		1 19 40835508 intron variant G/A snv 1.9E-02 0.700 1.000 1 2019 2019
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: rs13211840
rs13211840
UST
2 6 148791054 intron variant T/C snv 0.15 0.700 1.000 1 2016 2016
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