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: 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: 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: 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: 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: 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: 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: rs975334
rs975334
2 0.925 0.080 3 2804632 intron variant G/A snv 0.50 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: rs1048943
rs1048943
88 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 0.030 0.667 3 2007 2014
dbSNP: rs4986791
rs4986791
182 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 0.030 1.000 3 2010 2011
dbSNP: rs1042522
rs1042522
242 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 0.020 1.000 2 2007 2009
dbSNP: rs1052133
rs1052133
147 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 0.020 1.000 2 2007 2009
dbSNP: rs1131691014
rs1131691014
214 0.439 0.800 17 7676154 frameshift variant -/C ins 0.020 1.000 2 2007 2009
dbSNP: rs11887534
rs11887534
29 0.653 0.440 2 43839108 missense variant G/A;C snv 6.4E-06; 6.7E-02 0.020 1.000 2 2009 2011
dbSNP: rs20417
rs20417
57 0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 0.020 1.000 2 2009 2011
dbSNP: rs2695121
rs2695121
16 0.716 0.280 19 50377484 5 prime UTR variant T/C snv 0.70 0.020 < 0.001 2 2013 2014
dbSNP: rs878854066
rs878854066
213 0.439 0.800 17 7676153 missense variant GG/AC mnv 0.020 1.000 2 2007 2009