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: rs4148008
rs4148008
2 17 68879153 non coding transcript exon variant C/G snv 0.40 0.800 1.000 3 2010 2019
dbSNP: rs1373067
rs1373067
1 17 68905225 intron variant T/A;C snv 0.700 1.000 1 2017 2017
dbSNP: rs4148005
rs4148005
1 17 68886325 intron variant T/G snv 0.39 0.700 1.000 1 2019 2019