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: rs1561498701
rs1561498701
5 1.000 0.080 5 70925150 frameshift variant -/GGATTCCG delins 0.700 1.000 1 2013 2013
dbSNP: rs1561500885
rs1561500885
2 1.000 0.040 5 70946138 missense variant T/C snv 0.700 1.000 1 2007 2007