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: rs1219101402
rs1219101402
1 1.000 0.120 11 68365607 missense variant C/T snv 7.0E-06 0.700 1.000 5 2001 2008