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: rs369067856
rs369067856
2 0.925 0.080 1 55043945 missense variant C/A;T snv 3.2E-05 5.6E-05 0.010 1.000 1 2016 2016
dbSNP: rs374603772
rs374603772
9 0.776 0.160 1 55058630 missense variant C/T snv 4.4E-05 2.8E-05 0.010 1.000 1 2007 2007
dbSNP: rs775988212
rs775988212
2 0.925 0.080 1 55043976 missense variant T/C snv 1.2E-05 7.0E-06 0.010 1.000 1 2016 2016