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: rs16856247
rs16856247
2 2 168927903 intron variant C/T snv 6.6E-02 0.700 1.000 1 2011 2011
dbSNP: rs473351
rs473351
3 0.925 0.120 2 168923386 3 prime UTR variant T/A;C;G snv 0.700 1.000 1 2012 2012
dbSNP: rs475612
rs475612
1 2 168920236 intron variant T/C snv 0.73 0.700 1.000 1 2012 2012
dbSNP: rs485094
rs485094
1 2 168925843 intron variant A/C snv 0.73 0.700 1.000 1 2012 2012
dbSNP: rs486981
rs486981
1 2 168925639 intron variant A/G snv 0.73 0.700 1.000 1 2012 2012
dbSNP: rs494874
rs494874
1 2 168932796 3 prime UTR variant T/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs502570
rs502570
1 2 168918449 intron variant A/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs508506
rs508506
1 2 168928445 intron variant A/C snv 0.76 0.700 1.000 1 2012 2012
dbSNP: rs518598
rs518598
1 2 168920404 intron variant T/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs537183
rs537183
1 2 168918136 intron variant C/T snv 0.75 0.700 1.000 1 2012 2012
dbSNP: rs552976
rs552976
1 2 168934928 intron variant A/G snv 0.66 0.700 1.000 1 2012 2012
dbSNP: rs557462
rs557462
1 2 168921085 3 prime UTR variant C/T snv 0.77 0.700 1.000 1 2012 2012
dbSNP: rs563694
rs563694
2 2 168917561 intron variant C/A snv 0.75 0.700 1.000 1 2012 2012
dbSNP: rs566879
rs566879
1 2 168926699 intron variant A/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs569805
rs569805
2 1.000 0.040 2 168926370 intron variant A/T snv 0.73 0.700 1.000 1 2012 2012
dbSNP: rs569829
rs569829
1 2 168926359 intron variant T/C snv 0.77 0.700 1.000 1 2012 2012
dbSNP: rs575671
rs575671
1 2 168924308 intron variant A/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs578763
rs578763
1 2 168919850 intron variant G/T snv 0.72 0.700 1.000 1 2012 2012
dbSNP: rs579060
rs579060
1 2 168926529 intron variant G/C;T snv 0.700 1.000 1 2012 2012
dbSNP: rs580613
rs580613
1 2 168919630 intron variant T/A snv 0.72 0.700 1.000 1 2012 2012
dbSNP: rs580670
rs580670
1 2 168919611 intron variant T/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs853777
rs853777
1 2 168955707 intron variant T/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs853787
rs853787
2 2 168945742 intron variant G/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs853789
rs853789
4 2 168944978 intron variant A/G;T snv 0.75 0.700 1.000 1 2012 2012