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: rs8049607
rs8049607
1 16 11597897 intron variant T/C snv 0.51 0.800 1.000 3 2009 2019
dbSNP: rs735951
rs735951
1 16 11599680 intron variant G/A;C snv 0.800 1.000 1 2009 2019