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: rs442177
rs442177
5 4 87109109 intron variant G/T snv 0.56 0.800 1.000 5 2010 2019
dbSNP: rs236996
rs236996
2 4 87084051 intron variant G/A snv 0.43 0.800 1.000 2 2012 2017
dbSNP: rs2035403
rs2035403
2 4 87097839 intron variant A/G snv 0.35 0.700 1.000 2 2015 2018
dbSNP: rs1037814
rs1037814
3 4 87128698 intron variant T/C snv 0.60 0.700 1.000 1 2017 2017
dbSNP: rs1408
rs1408
2 4 87136201 3 prime UTR variant G/A snv 0.63 0.700 1.000 1 2018 2018
dbSNP: rs17605615
rs17605615
1 4 87075593 intron variant G/A snv 0.35 0.700 1.000 1 2019 2019
dbSNP: rs3775214
rs3775214
2 4 87102147 intron variant A/G snv 0.34 0.700 1.000 1 2012 2012
dbSNP: rs60695258
rs60695258
4 4 87101557 intron variant C/A;T snv 0.700 1.000 1 2019 2019