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: rs397516685
rs397516685
3 0.882 0.120 10 88939680 missense variant C/T snv 0.700 1.000 2 2009 2009
dbSNP: rs727502878
rs727502878
2 0.925 0.120 10 88939595 missense variant C/G snv 0.700 0