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: rs121908012
rs121908012
3 0.878 0.143 10 125815061 missense variant A/C,G snp 4.0E-06; 2.1E-04 2.9E-04 0.010 1.000 1 2011 2011
dbSNP: rs766814208
rs766814208
5 0.846 0.107 10 95823259 synonymous variant C/T snp 1.6E-05 0.010 1.000 1 1993 1993