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: rs201590781
rs201590781
1 1.000 0.160 15 27966798 missense variant C/T snv 5.6E-05 8.4E-05 0.010 1.000 1 2015 2015