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: rs145268310
rs145268310 		4 0.882 3 12269274 regulatory region variant G/C snv 9.9E-02 0.700 1.000 1 2019 2019
dbSNP: rs1530687
rs1530687
ARHGAP31
4 0.882 3 119395668 intron variant G/A snv 0.46 0.700 1.000 1 2019 2019
dbSNP: rs1549922
rs1549922 		4 0.882 5 159304540 intergenic variant G/A snv 0.56 0.700 1.000 1 2019 2019
dbSNP: rs1790588
rs1790588
CD226
4 0.882 18 69867948 intron variant T/C snv 0.55 0.700 1.000 1 2019 2019
dbSNP: rs1800601
rs1800601
NTRK1 ; SH2D2A
4 0.882 1 156815825 5 prime UTR variant G/A;T snv 0.67; 4.0E-06 0.700 1.000 1 2019 2019
dbSNP: rs191252491
rs191252491
ALDH2
4 0.882 12 111773070 intron variant A/T snv 7.1E-03 0.700 1.000 1 2019 2019
dbSNP: rs1921445
rs1921445 		4 0.882 3 106229671 intergenic variant A/C;G snv 0.700 1.000 1 2019 2019
dbSNP: rs2093816
rs2093816
LINC02341
4 0.882 13 42471900 intron variant C/T snv 0.47 0.700 1.000 1 2019 2019
dbSNP: rs2181622
rs2181622
LINC02649 ; LINC02656
4 0.882 10 6349099 intron variant G/A snv 0.59 0.700 1.000 1 2019 2019
dbSNP: rs221781
rs221781 		4 0.882 7 100698285 upstream gene variant A/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs240753
rs240753
LOC105372548
4 0.882 20 17881170 intergenic variant T/C snv 0.43 0.700 1.000 1 2019 2019
dbSNP: rs28583049
rs28583049
LOC105374033
4 0.882 3 108724568 downstream gene variant T/C snv 0.17 0.700 1.000 1 2019 2019
dbSNP: rs35776863
rs35776863
NEURL4
4 0.882 17 7323638 intron variant G/A snv 0.14 0.14 0.700 1.000 1 2019 2019
dbSNP: rs391851
rs391851 		4 0.882 5 103342219 intergenic variant A/C;G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs4761587
rs4761587
PLXNC1
4 0.882 12 94158023 intron variant A/G snv 0.78 0.700 1.000 1 2019 2019
dbSNP: rs56817615
rs56817615
CLNK
4 0.882 4 10717222 intergenic variant A/G snv 0.42 0.700 1.000 1 2019 2019
dbSNP: rs57791671
rs57791671 		4 0.882 3 121889586 upstream gene variant T/A snv 0.38 0.700 1.000 1 2019 2019
dbSNP: rs67927699
rs67927699
PUS10
4 0.882 2 60960280 intron variant G/C;T snv 0.700 1.000 1 2019 2019
dbSNP: rs72920202
rs72920202
JAK1
4 0.882 1 64895266 intron variant A/T snv 0.15 0.700 1.000 1 2019 2019
dbSNP: rs7655915
rs7655915
LOC107986195
4 0.882 4 148712316 intron variant C/T snv 0.22 0.700 1.000 1 2019 2019
dbSNP: rs773107
rs773107
RAB5B
4 0.882 12 55975722 intron variant A/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs8061370
rs8061370
RMI2 ; LOC105371082
4 0.882 16 11364614 intron variant A/C;T snv 0.700 1.000 1 2019 2019
dbSNP: rs865488
rs865488
TG
4 0.882 8 132926377 intron variant C/T snv 0.67 0.700 1.000 1 2019 2019
dbSNP: rs9356551
rs9356551 		4 0.882 6 166986857 intron variant T/C snv 0.42 0.700 1.000 1 2019 2019
dbSNP: rs9683415
rs9683415 		4 0.882 4 40290296 regulatory region variant A/G snv 0.71 0.700 1.000 1 2019 2019