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: rs3134945
rs3134945
3 0.827 0.240 6 32178715 intron variant C/A snv 0.18 0.700 1.000 3 2007 2011
dbSNP: rs3134943
rs3134943
3 0.882 0.240 6 32179984 intron variant T/A;C snv 0.89 0.700 1.000 2 2007 2009
dbSNP: rs1269839
rs1269839
1 1.000 0.120 6 32169153 3 prime UTR variant G/A;T snv 0.700 1.000 1 2011 2011
dbSNP: rs3130284
rs3130284
2 0.925 0.120 6 32172710 intron variant T/C snv 0.18 0.700 1.000 1 2011 2011
dbSNP: rs3130348
rs3130348
1 1.000 0.120 6 32172500 intron variant C/A snv 0.18 0.700 1.000 1 2011 2011
dbSNP: rs3130349
rs3130349
1 1.000 0.120 6 32179919 synonymous variant G/A;C snv 0.14; 4.0E-06 0.700 1.000 1 2011 2011
dbSNP: rs3131297
rs3131297
1 1.000 0.120 6 32173228 intron variant A/T snv 0.18 0.700 1.000 1 2011 2011
dbSNP: rs3132965
rs3132965
1 1.000 0.120 6 32179220 intron variant A/G snv 0.18 0.700 1.000 1 2011 2011
dbSNP: rs3134946
rs3134946
1 1.000 0.120 6 32178216 upstream gene variant C/G snv 0.18 0.700 1.000 1 2011 2011
dbSNP: rs3134947
rs3134947
2 0.925 0.120 6 32177428 intron variant C/T snv 0.18 0.700 1.000 1 2011 2011