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: rs2035403
rs2035403
2 4 87097839 intron variant A/G snv 0.35 0.700 1.000 1 2018 2018
dbSNP: rs442177
rs442177
5 4 87109109 intron variant G/T snv 0.56 0.700 1.000 1 2018 2018
dbSNP: rs60695258
rs60695258
4 4 87101557 intron variant C/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs7660883
rs7660883
2 4 87061724 intron variant C/A;G;T snv 0.700 1.000 1 2017 2017