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: rs1252688154
rs1252688154
1 1.000 0.080 1 155187520 missense variant C/T snv 4.0E-06 0.010 1.000 1 2014 2014
dbSNP: rs375294990
rs375294990
1 1.000 0.080 1 155192150 missense variant G/C snv 8.0E-06 5.6E-05 0.010 1.000 1 2014 2014