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: rs1419040
rs1419040 		1 1.000 0.080 X 51609183 intergenic variant G/A snv 0.700 1.000 1 2008 2008
dbSNP: rs1447293
rs1447293
CASC8
1 1.000 0.080 8 127460075 intron variant C/T snv 0.48 0.700 1.000 1 2008 2008
dbSNP: rs147739031
rs147739031
CSMD1
1 1.000 0.080 8 3389886 intron variant A/C;G snv 0.700 1.000 1 2014 2014
dbSNP: rs1543175
rs1543175
LSAMP
1 1.000 0.080 3 116668062 intron variant G/A snv 0.45 0.700 1.000 1 2011 2011
dbSNP: rs16824376
rs16824376
PLCL1
1 1.000 0.080 2 197819618 intron variant C/T snv 0.19 0.700 1.000 1 2012 2012
dbSNP: rs16972648
rs16972648
CFAP161
1 1.000 0.080 15 81016085 intron variant G/A;C snv 0.700 1.000 1 2011 2011
dbSNP: rs1851779
rs1851779
BOLL
1 1.000 0.080 2 197782384 intron variant C/T snv 0.19 0.700 1.000 1 2012 2012
dbSNP: rs2185710
rs2185710
LOC107986636
1 1.000 0.080 6 113055846 intron variant A/G snv 0.51 0.700 1.000 1 2014 2014
dbSNP: rs2293255
rs2293255
BOLL
1 1.000 0.080 2 197756782 intron variant T/C snv 0.20 0.700 1.000 1 2012 2012
dbSNP: rs2611512
rs2611512 		1 1.000 0.080 10 46080288 regulatory region variant T/C snv 0.49 0.700 1.000 1 2008 2008
dbSNP: rs365586
rs365586 		1 1.000 0.080 14 39984510 intron variant G/A;C snv 0.38 0.700 1.000 1 2011 2011
dbSNP: rs395080
rs395080 		1 1.000 0.080 14 39982929 intron variant C/A;T snv 0.700 1.000 1 2011 2011
dbSNP: rs417245
rs417245 		1 1.000 0.080 14 39978496 intron variant T/C snv 0.39 0.700 1.000 1 2011 2011
dbSNP: rs4604628
rs4604628 		1 1.000 0.080 X 51644318 intergenic variant C/G;T snv 0.700 1.000 1 2008 2008
dbSNP: rs4872171
rs4872171
LOC107986930
1 1.000 0.080 8 23656776 intergenic variant A/G;T snv 0.48 0.700 1.000 1 2012 2012
dbSNP: rs4872172
rs4872172
LOC107986930
1 1.000 0.080 8 23656830 intergenic variant T/A;C;G snv 0.700 1.000 1 2012 2012
dbSNP: rs4999155
rs4999155 		1 1.000 0.080 9 81848028 regulatory region variant C/T snv 0.11 0.700 1.000 1 2012 2012
dbSNP: rs5991735
rs5991735
MAGED1
1 1.000 0.080 X 51809788 intron variant G/A;C snv 0.700 1.000 1 2008 2008
dbSNP: rs6008813
rs6008813
CELSR1
1 1.000 0.080 22 46416688 intron variant G/A snv 0.26 0.700 1.000 1 2014 2014
dbSNP: rs61749035
rs61749035
PCDHGA2 ; PCDHGA1
1 1.000 0.080 5 141339183 missense variant G/T snv 3.4E-03 1.4E-02 0.700 1.000 1 2014 2014
dbSNP: rs62477096
rs62477096
LOC101928283
1 1.000 0.080 7 125296388 intron variant A/G snv 0.19 0.700 1.000 1 2014 2014
dbSNP: rs629242
rs629242
CRACD
1 1.000 0.080 4 56276871 intron variant C/T snv 0.25 0.700 1.000 1 2007 2007
dbSNP: rs6465654
rs6465654
LMTK2
1 1.000 0.080 7 98156970 intron variant G/A snv 0.36 0.700 1.000 1 2008 2008
dbSNP: rs66504230
rs66504230 		1 1.000 0.080 6 86161726 intergenic variant T/C snv 0.11 0.700 1.000 1 2014 2014
dbSNP: rs6707521
rs6707521
PLCL1
1 1.000 0.080 2 197848507 intron variant G/A snv 0.18 0.700 1.000 1 2012 2012