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: rs2273061
rs2273061
3 1.000 0.080 20 10658895 intron variant G/A snv 0.46 0.700 1.000 1 2010 2010
dbSNP: rs3790160
rs3790160
2 20 10659340 intron variant T/C snv 0.54 0.700 1.000 1 2012 2012
dbSNP: rs6040063
rs6040063
1 20 10660229 intron variant A/G snv 0.54 0.700 1.000 1 2018 2018