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: rs1934697
rs1934697
1 10 80353117 intron variant C/T snv 0.50 0.700 1.000 1 2019 2019
dbSNP: rs35505876
rs35505876
1 10 80363511 intron variant -/G;GT;GTT;GTTT;GTTTT ins 0.700 1.000 1 2019 2019