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: rs10744773
rs10744773
1 12 111649006 intron variant C/A snv 0.36 0.700 1.000 1 2012 2012
dbSNP: rs3742001
rs3742001
1 12 111665344 intron variant C/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs7136874
rs7136874
1 12 111675854 intron variant C/T snv 0.36 0.700 1.000 1 2012 2012
dbSNP: rs7977828
rs7977828
1 12 111656962 intron variant A/G snv 0.27 0.700 1.000 1 2012 2012
dbSNP: rs847895
rs847895
1 12 111680772 intron variant T/C snv 0.18 0.700 1.000 1 2012 2012