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: rs161870
rs161870
2 0.925 0.160 5 7878079 synonymous variant T/C snv 0.18 0.21 0.010 1.000 1 2013 2013
dbSNP: rs1801394
rs1801394
101 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 0.010 1.000 1 2004 2004