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: rs142014203
rs142014203
1 1.000 0.036 8 62346358 intron variant T/G snp 1.9E-02 0.700 1 2014 2014
dbSNP: rs1445130
rs1445130
1 1.000 0.036 2 18653385 intergenic variant A/G snp 0.11 0.700 1 2014 2014
dbSNP: rs4680
rs4680
155 0.484 0.821 22 19963748 missense variant G/A snp 0.46 0.45 0.030 1.000 3 2011 2018
dbSNP: rs1042571
rs1042571
4 0.878 0.107 2 25161018 3 prime UTR variant G/A snp 0.15 0.010 1.000 1 2015 2015
dbSNP: rs1049353
rs1049353
26 0.657 0.464 6 88143916 synonymous variant C/T snp 0.21 0.20 0.010 1.000 1 2010 2010
dbSNP: rs13338499
rs13338499
2 0.923 0.036 16 67486220 intron variant A/G,T snp 0.27 0.010 1.000 1 2015 2015
dbSNP: rs1800497
rs1800497
36 0.662 0.250 11 113400106 missense variant G/A snp 0.26 0.26 0.010 1.000 1 2013 2013
dbSNP: rs4633
rs4633
13 0.756 0.214 22 19962712 synonymous variant C/T snp 0.46 0.46 0.010 1.000 1 2011 2011
dbSNP: rs4818
rs4818
16 0.734 0.286 22 19963684 synonymous variant C/G,T snp 0.34 0.32 0.010 1.000 1 2011 2011
dbSNP: rs495225
rs495225
3 0.923 0.036 3 172448243 synonymous variant G/A,C,T snp 0.66 0.63 0.010 1.000 1 2007 2007
dbSNP: rs53576
rs53576
23 0.692 0.107 3 8762685 intron variant A/G,T snp 0.67 0.010 1.000 1 2015 2015
dbSNP: rs554073050
rs554073050
CCK
3 0.923 0.036 3 42263460 synonymous variant G/A snp 1.2E-05 0.010 1.000 1 2007 2007
dbSNP: rs6265
rs6265
171 0.463 0.679 11 27658369 missense variant C/T snp 0.19 0.15 0.010 1.000 1 2008 2008
dbSNP: rs6296
rs6296
12 0.769 0.071 6 77462543 synonymous variant C/G snp 0.31 0.27 0.010 1.000 1 2001 2001
dbSNP: rs696217
rs696217
24 0.685 0.536 3 10289773 missense variant G/T snp 8.8E-02 7.2E-02 0.010 1.000 1 2007 2007
dbSNP: rs759834365
rs759834365
157 0.471 0.679 11 27658456 missense variant C/T snp 1.2E-05 0.010 1.000 1 2008 2008