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: rs1132200
rs1132200
2 0.925 0.160 3 119431989 missense variant C/T snv 0.12 0.11 0.710 0.500 1 2011 2012