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: rs104894578
rs104894578
6 0.807 0.280 17 70175691 missense variant C/T snv 0.010 1.000 1 2006 2006