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: rs3849942
rs3849942
2 0.776 0.200 9 27543283 non coding transcript exon variant T/A;C snv 0.870 1.000 5 2009 2018
dbSNP: rs2814707
rs2814707
2 0.882 0.120 9 27536399 non coding transcript exon variant C/G;T snv 0.830 1.000 3 2009 2014
dbSNP: rs10122902
rs10122902
1 1.000 0.080 9 27556782 synonymous variant G/A snv 0.24 0.21 0.800 1.000 1 2010 2010
dbSNP: rs774359
rs774359
1 1.000 0.080 9 27561051 3 prime UTR variant T/C snv 0.23 0.700 1.000 2 2010 2013
dbSNP: rs10757665
rs10757665
1 1.000 0.080 9 27557921 intron variant T/C snv 0.20 0.700 1.000 1 2013 2013
dbSNP: rs10812611
rs10812611
1 1.000 0.080 9 27542263 non coding transcript exon variant C/T snv 0.42 0.700 1.000 1 2013 2013
dbSNP: rs10967976
rs10967976
1 1.000 0.080 9 27544945 intron variant G/A;C snv 0.700 1.000 1 2013 2013
dbSNP: rs12349820
rs12349820
1 1.000 0.080 9 27553878 intron variant T/C snv 0.20 0.700 1.000 1 2013 2013
dbSNP: rs1565948
rs1565948
1 1.000 0.080 9 27559735 non coding transcript exon variant G/A snv 0.43 0.700 1.000 1 2013 2013
dbSNP: rs2282240
rs2282240
1 1.000 0.080 9 27572636 intron variant C/T snv 0.23 0.700 1.000 1 2013 2013
dbSNP: rs2282241
rs2282241
1 1.000 0.080 9 27572257 intron variant C/A snv 0.38 0.700 1.000 1 2013 2013
dbSNP: rs60242496
rs60242496
1 1.000 0.080 9 27572636 intron variant -/GGAAAGTGCAGGACCTCCCTCCTG delins 0.700 1.000 1 2013 2013
dbSNP: rs774357
rs774357
1 1.000 0.080 9 27559837 non coding transcript exon variant G/A snv 0.21 0.700 1.000 1 2013 2013