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: rs4362633
rs4362633
1 20 17464490 non coding transcript exon variant A/C snv 0.10 0.700 1.000 1 2012 2012
dbSNP: rs6044834
rs6044834
1 20 17455828 intron variant T/G snv 0.15 0.700 1.000 1 2012 2012