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: rs724577
rs724577
3 4 17991787 intron variant A/C snv 0.71 0.800 1.000 1 2013 2013
dbSNP: rs2174633
rs2174633
1 4 17916158 intron variant A/C snv 0.70 0.700 1.000 1 2019 2019
dbSNP: rs4144829
rs4144829
1 4 17902031 intron variant C/T snv 0.72 0.700 1.000 1 2019 2019
dbSNP: rs925098
rs925098
3 4 17918188 intron variant G/A snv 0.70 0.700 1.000 1 2016 2016