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: rs10504229
rs10504229
LINC00588
1 1.000 0.080 8 57283936 intron variant A/G snv 0.16 0.700 1.000 1 2016 2016
dbSNP: rs10774547
rs10774547 		3 0.925 0.120 12 120424913 intergenic variant T/C snv 0.39 0.700 1.000 1 2014 2014
dbSNP: rs12121864
rs12121864 		1 1.000 0.080 1 9145273 downstream gene variant C/A snv 5.2E-02 0.700 1.000 1 2016 2016
dbSNP: rs1711745
rs1711745
INIP
3 0.925 0.120 9 112690629 intron variant C/A snv 0.13 0.700 1.000 1 2014 2014
dbSNP: rs3787751
rs3787751
HLCS
1 1.000 0.080 21 36787862 intron variant T/A;C snv 0.700 1.000 1 2016 2016
dbSNP: rs59197085
rs59197085
CCDC136
3 0.925 0.120 7 128820702 intron variant G/A snv 9.9E-02 0.700 1.000 1 2014 2014
dbSNP: rs5995177
rs5995177
RBFOX2
2 0.925 0.120 22 35913505 intron variant G/A;C snv 0.700 1.000 1 2014 2014
dbSNP: rs2710102
rs2710102
CNTNAP2
12 0.790 0.120 7 147877298 intron variant A/G;T snv 0.010 1.000 1 2011 2011
dbSNP: rs397514679
rs397514679
SYN1
9 0.790 0.200 X 47574321 stop gained G/A snv 0.010 1.000 1 2015 2015