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: rs5767700
rs5767700
1 22 46216775 intron variant T/C;G snv 0.010 1.000 1 2015 2015
dbSNP: rs5767743
rs5767743
1 22 46226097 intron variant T/C snv 0.36 0.010 1.000 1 2015 2015