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: rs893001
rs893001
1 18 69849610 intron variant A/C snv 0.18 0.800 1.000 2 2009 2012
dbSNP: rs12969657
rs12969657
1 18 69869260 intron variant C/T snv 0.41 0.800 1.000 1 2011 2011
dbSNP: rs201800621
rs201800621
1 18 69849609 intron variant G/A;C snv 0.700 1.000 2 2009 2012
dbSNP: rs75761474
rs75761474
1 18 69849610 intron variant A/- del 0.53 0.700 1.000 2 2009 2012
dbSNP: rs1823778
rs1823778
1 18 69934400 intron variant G/C snv 0.67 0.700 1.000 1 2016 2016
dbSNP: rs1865761
rs1865761
1 18 69872156 intron variant T/C snv 0.41 0.700 1.000 1 2016 2016