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: rs104894060
rs104894060
3 0.882 0.120 8 1780316 missense variant C/T snv 3.2E-05 7.0E-06 0.800 1.000 8 2004 2016