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: rs35479735
rs35479735
1 1.000 0.040 2 156326700 intron variant C/- delins 0.71 0.79 0.020 0.500 2 2017 2017
dbSNP: rs1453063924
rs1453063924
1 1.000 0.040 2 156329978 missense variant C/T snv 4.0E-06 0.010 1.000 1 2005 2005