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: rs1656402
rs1656402
1 1.000 0.080 2 232561816 intron variant C/T snv 0.31 0.700 1.000 1 2011 2011