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: rs121909067
rs121909067
2 0.925 0.120 18 3456525 missense variant C/G snv 0.010 1.000 1 2007 2007
dbSNP: rs1315861554
rs1315861554
2 0.925 0.120 18 3457392 missense variant C/T snv 4.0E-06 0.010 1.000 1 2002 2002
dbSNP: rs199580307
rs199580307
3 0.882 0.160 18 3457498 missense variant T/C snv 2.6E-04 1.1E-04 0.010 1.000 1 2006 2006
dbSNP: rs970137214
rs970137214
1 1.000 0.120 18 3457798 missense variant C/T snv 8.0E-06 2.1E-05 0.010 1.000 1 2007 2007