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: rs121917867
rs121917867
MIP
4 0.846 0.071 12 56453703 missense variant G/A,C snp 4.0E-05 0.010 1.000 1 2001 2001
dbSNP: rs121917869
rs121917869
MIP
4 0.846 0.071 12 56453715 missense variant T/C,G snp 0.010 1.000 1 2001 2001