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: rs11545664
rs11545664
ENG
4 0.925 0.120 9 127843106 synonymous variant C/T snv 9.3E-02 0.14 0.010 < 0.001 1 2015 2015
dbSNP: rs201393380
rs201393380
4 0.925 0.120 9 127825767 missense variant C/G snv 1.3E-04 7.8E-04 0.010 < 0.001 1 2015 2015