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: rs10205219
rs10205219
2 0.925 0.120 2 27345698 intron variant T/A;C snv 0.700 1.000 2 2010 2013
dbSNP: rs1049817
rs1049817
3 0.925 0.120 2 27328100 synonymous variant A/G snv 0.42 0.48 0.700 1.000 2 2010 2013
dbSNP: rs11684134
rs11684134
2 0.925 0.120 2 27335385 synonymous variant A/G snv 0.44 0.44 0.700 1.000 2 2010 2013
dbSNP: rs3739095
rs3739095
2 0.925 0.120 2 27333854 intron variant G/A snv 0.55 0.700 1.000 2 2010 2013
dbSNP: rs4665969
rs4665969
2 0.925 0.120 2 27352086 intron variant T/C snv 0.39 0.700 1.000 2 2010 2013
dbSNP: rs6743819
rs6743819
2 0.925 0.120 2 27344540 intron variant G/C;T snv 0.700 1.000 2 2010 2013
dbSNP: rs6760828
rs6760828
2 0.925 0.120 2 27356364 5 prime UTR variant T/C snv 0.47 0.700 1.000 2 2010 2013
dbSNP: rs11689803
rs11689803
2 0.925 0.120 2 27343653 intron variant T/A snv 0.19 0.700 1.000 1 2013 2013