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: rs10119066
rs10119066 		1 1.000 0.120 9 7509895 intergenic variant G/C;T snv 0.700 1.000 1 2015 2015
dbSNP: rs11580861
rs11580861 		1 1.000 0.120 1 195026001 intergenic variant C/T snv 2.4E-02 0.700 1.000 1 2015 2015
dbSNP: rs12725009
rs12725009
MEGF6
1 1.000 0.120 1 3497433 intron variant G/A snv 9.9E-03 0.700 1.000 1 2015 2015
dbSNP: rs410285
rs410285
PRAMENP
1 1.000 0.120 22 22027370 intron variant A/G;T snv 0.700 1.000 1 2015 2015
dbSNP: rs62505227
rs62505227 		1 1.000 0.120 8 40429730 regulatory region variant G/A snv 6.7E-02 0.700 1.000 1 2015 2015
dbSNP: rs78315000
rs78315000
PREX2
1 1.000 0.120 8 68190823 intron variant A/G snv 3.3E-02 0.700 1.000 1 2015 2015
dbSNP: rs9291768
rs9291768 		1 1.000 0.120 5 51421959 intergenic variant C/T snv 0.39 0.700 1.000 1 2015 2015