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: rs397514668
rs397514668
1 1.000 0.080 20 35434276 missense variant C/T snv 4.0E-06 0.810 1.000 3 2005 2012
dbSNP: rs28936683
rs28936683
3 0.882 0.080 20 35434093 missense variant A/G snv 7.0E-06 0.800 0