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: rs6893300
rs6893300
1 5 179708814 intron variant C/A snv 0.24 0.800 1.000 1 2014 2014
dbSNP: rs7735702
rs7735702
1 5 179705611 intron variant T/A snv 0.26 0.700 1.000 1 2014 2014