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: rs34325700
rs34325700 		1 8 42673524 intergenic variant -/A delins 0.700 1.000 1 2010 2010
dbSNP: rs200049096
rs200049096
HYKK
1 15 78510715 intron variant -/T delins 1.4E-05 0.700 1.000 3 2010 2010
dbSNP: rs17486278
rs17486278
CHRNA5
9 0.827 0.120 15 78575140 intron variant A/C snv 0.32 0.700 1.000 2 2010 2010
dbSNP: rs1979905
rs1979905
PSMA4
1 15 78550032 3 prime UTR variant A/C snv 0.66 0.700 1.000 2 2010 2010
dbSNP: rs2656052
rs2656052
IREB2
3 15 78448590 intron variant A/C snv 0.36 0.700 1.000 2 2010 2010
dbSNP: rs6495314
rs6495314
CHRNB4 ; LOC112268142
4 0.925 0.080 15 78668187 intron variant A/C snv 0.35 0.700 1.000 2 2010 2010
dbSNP: rs1028936
rs1028936
HECTD2-AS1
1 10 91590040 regulatory region variant A/C snv 0.18 0.700 1.000 1 2012 2012
dbSNP: rs10919388
rs10919388 		4 1 170403362 intergenic variant A/C snv 0.71 0.700 1.000 1 2017 2017
dbSNP: rs11072811
rs11072811
MORF4L1
2 1.000 0.040 15 78839988 intron variant A/C snv 0.51 0.700 1.000 1 2010 2010
dbSNP: rs12854631
rs12854631 		2 X 58297412 intergenic variant A/C snv 2.7E-02 0.700 1.000 1 2015 2015
dbSNP: rs139214349
rs139214349 		2 4 29168543 intron variant A/C snv 1.4E-02 0.700 1.000 1 2015 2015
dbSNP: rs1396618
rs1396618
NRXN3
1 14 78825561 intron variant A/C snv 9.9E-02 0.700 1.000 1 2010 2010
dbSNP: rs147168872
rs147168872
SOS2
2 14 50173277 intron variant A/C snv 5.0E-03 0.700 1.000 1 2015 2015
dbSNP: rs1856293
rs1856293 		2 6 133159801 intergenic variant A/C snv 0.56 0.700 1.000 1 2017 2017
dbSNP: rs6437061
rs6437061
DIS3L2
3 2 232320342 intron variant A/C snv 0.56 0.700 1.000 1 2017 2017
dbSNP: rs7017612
rs7017612 		1 8 42744102 regulatory region variant A/C snv 0.36 0.700 1.000 1 2010 2010
dbSNP: rs72724928
rs72724928
LINGO2
2 9 28024196 intron variant A/C snv 3.3E-02 0.700 1.000 1 2015 2015
dbSNP: rs72923818
rs72923818
DYM
2 18 49157384 intron variant A/C snv 4.0E-02 0.700 1.000 1 2015 2015
dbSNP: rs7506051
rs7506051
ZNF407
1 18 74589381 downstream gene variant A/C snv 0.72 0.700 1.000 1 2010 2010
dbSNP: rs7837296
rs7837296 		1 8 42671751 intergenic variant A/C snv 0.70 0.700 1.000 1 2010 2010
dbSNP: rs189798510
rs189798510 		2 17 14811500 intergenic variant A/C;G snv 0.700 1.000 1 2015 2015
dbSNP: rs215601
rs215601
PDE1C
1 7 32294309 intron variant A/C;G snv 0.700 1.000 1 2010 2010
dbSNP: rs2945731
rs2945731 		2 8 133627845 intergenic variant A/C;G snv 4.9E-02 0.700 1.000 1 2015 2015
dbSNP: rs4947642
rs4947642 		3 7 51797912 intergenic variant A/C;G snv 0.700 1.000 1 2015 2015
dbSNP: rs6090583
rs6090583
EYA2
3 20 46930192 intron variant A/C;G snv 0.700 1.000 1 2017 2017