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: rs8038465
rs8038465
1 15 73685996 intron variant C/T snv 0.31 0.800 1.000 1 2011 2011
dbSNP: rs12594627
rs12594627
1 15 73693923 intron variant G/T snv 0.35 0.700 1.000 1 2018 2018