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: rs11082960
rs11082960
DCC
1 1.000 0.080 18 52999470 intron variant G/T snv 0.72 0.700 1.000 1 2012 2012
dbSNP: rs2071011
rs2071011
CCKAR
1 1.000 0.080 4 26489811 intron variant C/G;T snv 0.010 1.000 1 2013 2013
dbSNP: rs3822222
rs3822222
CCKAR
1 1.000 0.080 4 26489030 intron variant G/A snv 0.14 0.010 1.000 1 2013 2013
dbSNP: rs4077283
rs4077283
DCC
1 1.000 0.080 18 53019949 intron variant G/A snv 0.72 0.700 1.000 1 2012 2012
dbSNP: rs4078289
rs4078289
DCC
1 1.000 0.080 18 53020735 intron variant A/G snv 0.75 0.700 1.000 1 2012 2012
dbSNP: rs4940234
rs4940234
DCC
1 1.000 0.080 18 53012182 intron variant C/A snv 0.72 0.700 1.000 1 2012 2012
dbSNP: rs7233818
rs7233818
DCC
1 1.000 0.080 18 53009439 intron variant T/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs7504512
rs7504512
DCC
1 1.000 0.080 18 53003267 intron variant G/A snv 0.73 0.700 1.000 1 2012 2012
dbSNP: rs7504750
rs7504750
DCC
1 1.000 0.080 18 53021270 intron variant C/A snv 0.73 0.700 1.000 1 2012 2012
dbSNP: rs7506454
rs7506454
DCC
1 1.000 0.080 18 53007301 intron variant G/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs7506663
rs7506663
DCC
1 1.000 0.080 18 52993157 intron variant T/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs7507060
rs7507060
DCC
1 1.000 0.080 18 52999187 intron variant C/T snv 0.73 0.700 1.000 1 2012 2012
dbSNP: rs915889
rs915889
CCKAR
1 1.000 0.080 4 26484572 intron variant G/A snv 0.15 0.010 1.000 1 2013 2013
dbSNP: rs9304437
rs9304437
DCC
1 1.000 0.080 18 52995196 intron variant T/G snv 0.73 0.700 1.000 1 2012 2012
dbSNP: rs9944713
rs9944713
DCC
1 1.000 0.080 18 53008042 intron variant C/A snv 0.72 0.700 1.000 1 2012 2012
dbSNP: rs9957080
rs9957080
DCC
1 1.000 0.080 18 52994363 intron variant G/T snv 0.73 0.700 1.000 1 2012 2012
dbSNP: rs1800855
rs1800855
CCKAR
2 0.925 0.120 4 26489495 intron variant A/G;T snv 0.27 0.010 1.000 1 2013 2013
dbSNP: rs975334
rs975334
CNTN4
2 0.925 0.080 3 2804632 intron variant G/A snv 0.50 0.700 1.000 1 2012 2012
dbSNP: rs4078288
rs4078288
DCC
3 0.882 0.120 18 53020881 intron variant G/A snv 0.73 0.700 1.000 1 2012 2012
dbSNP: rs7504990
rs7504990
DCC
4 0.851 0.120 18 52991406 intron variant T/C snv 0.73 0.700 1.000 1 2012 2012
dbSNP: rs1157
rs1157
ALCAM
7 0.790 0.080 3 105576617 3 prime UTR variant G/A snv 0.16 0.010 1.000 1 2016 2016
dbSNP: rs1169803481
rs1169803481
EGFR
7 0.807 0.160 7 55198851 missense variant A/G snv 4.0E-06 0.010 1.000 1 2015 2015
dbSNP: rs13959
rs13959
ALDH1A1
7 0.790 0.080 9 72930966 synonymous variant G/A snv 0.48 0.42 0.010 1.000 1 2016 2016
dbSNP: rs1444424830
rs1444424830
FASTK
7 0.790 0.080 7 151078923 missense variant C/T snv 4.6E-06 7.0E-06 0.010 < 0.001 1 2014 2014
dbSNP: rs4595552
rs4595552 		7 0.790 0.080 11 125865825 intergenic variant C/G;T snv 0.010 1.000 1 2016 2016