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: rs4128725
rs4128725
1 1 159436169 intron variant T/C;G snv 0.700 1.000 2 2007 2012
dbSNP: rs10908716
rs10908716
1 1 159406553 intron variant A/G snv 0.10 0.700 1.000 1 2012 2012
dbSNP: rs10908717
rs10908717
1 1 159406562 intron variant C/A snv 0.10 0.700 1.000 1 2012 2012
dbSNP: rs11265186
rs11265186
1 1 159406113 non coding transcript exon variant C/T snv 0.11 0.700 1.000 1 2012 2012
dbSNP: rs11265187
rs11265187
1 1 159408804 intron variant C/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs11265190
rs11265190
2 1 159421611 intron variant G/A snv 0.47 0.700 1.000 1 2012 2012
dbSNP: rs11265191
rs11265191
2 1 159430569 intron variant C/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs11265193
rs11265193
1 1 159431866 intron variant G/T snv 0.11 0.700 1.000 1 2012 2012
dbSNP: rs11265194
rs11265194
1 1 159433899 intron variant G/T snv 0.63 0.700 1.000 1 2012 2012
dbSNP: rs12034969
rs12034969
2 1 159415154 intron variant T/C snv 0.46 0.700 1.000 1 2012 2012
dbSNP: rs12048482
rs12048482
1 1 159440067 missense variant A/G snv 0.56 0.57 0.700 1.000 1 2012 2012
dbSNP: rs12118201
rs12118201
1 1 159427151 intron variant C/T snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs12118628
rs12118628
1 1 159440094 missense variant G/A snv 0.14 0.11 0.700 1.000 1 2012 2012
dbSNP: rs12145616
rs12145616
1 1 159439689 intron variant T/A;G snv 0.700 1.000 1 2012 2012
dbSNP: rs3122633
rs3122633
1 1 159407668 intron variant T/C snv 0.37 0.700 1.000 1 2012 2012
dbSNP: rs4492615
rs4492615
1 1 159422073 intron variant T/C snv 0.11 0.700 1.000 1 2012 2012
dbSNP: rs4656236
rs4656236
2 1 159441185 3 prime UTR variant G/A snv 0.18 0.700 1.000 1 2012 2012