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: rs1366594
rs1366594
3 5 89080244 intron variant A/C snv 0.57 0.800 1.000 3 2009 2018
dbSNP: rs10037512
rs10037512
3 5 89058858 intron variant T/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs6894139
rs6894139
3 5 89031965 non coding transcript exon variant T/G snv 0.57 0.700 1.000 1 2014 2014
dbSNP: rs7725337
rs7725337
1 5 89095690 intron variant T/C snv 0.43 0.700 1.000 1 2018 2018
dbSNP: rs7728694
rs7728694
1 5 88992524 intron variant G/A;T snv 0.58 0.700 1.000 1 2018 2018