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: rs13170232
rs13170232
1 1.000 0.040 5 153519972 intron variant T/A snv 9.5E-02 0.700 1.000 1 2015 2015
dbSNP: rs7727515
rs7727515
1 1.000 0.040 5 153512744 intron variant G/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs1428920
rs1428920
1 1.000 0.040 5 153497448 intron variant C/T snv 0.37 0.010 1.000 1 2012 2012
dbSNP: rs2926835
rs2926835
1 1.000 0.040 5 153809370 intron variant T/A;C snv 0.010 1.000 1 2012 2012