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: rs1894633
rs1894633
1 1 172361919 intron variant A/G snv 0.38 0.700 1.000 1 2017 2017
dbSNP: rs2001129
rs2001129
1 1 172364108 intron variant T/A;G snv 0.700 1.000 1 2017 2017