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: rs17132261
rs17132261
TMEM232
2 1.000 0.080 5 110672513 intron variant C/T snv 4.8E-02 0.800 1.000 1 2009 2009
dbSNP: rs7910620
rs7910620
GRID1
1 10 86087202 intron variant C/G;T snv 0.800 1.000 1 2009 2009
dbSNP: rs89107
rs89107
SLC35F1
1 6 118256880 intron variant G/A snv 0.46 0.800 1.000 1 2009 2009
dbSNP: rs1379659
rs1379659
SLIT2
2 4 20619060 3 prime UTR variant G/A snv 0.85 0.86 0.700 1.000 1 2007 2007
dbSNP: rs1436109
rs1436109
NCAM1
3 1.000 0.080 11 113120896 intron variant G/T snv 8.5E-02 0.700 1.000 1 2011 2011
dbSNP: rs3814219
rs3814219
STN1
1 10 103887337 intron variant G/A snv 0.22 0.700 1.000 1 2007 2007