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: rs2303369
rs2303369
3 0.925 0.120 2 27492549 intron variant C/T snv 0.38 0.800 1.000 1 2012 2012
dbSNP: rs704795
rs704795
3 0.925 0.120 2 27493627 intron variant G/A snv 0.46 0.700 1.000 1 2015 2015
dbSNP: rs780088
rs780088
1 2 27493137 intron variant T/C snv 0.46 0.700 1.000 1 2019 2019