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: rs1801394
rs1801394
101 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.040 1.000 4 2007 2016
dbSNP: rs372359132
rs372359132
5 0.827 0.160 5 7878203 missense variant A/G snv 4.0E-06 2.1E-05 0.010 1.000 1 2007 2007