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: rs104893855
rs104893855
4 0.851 0.160 4 41747479 missense variant C/A snv 0.010 1.000 1 2014 2014
dbSNP: rs104893856
rs104893856
6 0.827 0.080 4 41746162 missense variant C/T snv 0.010 < 0.001 1 2006 2006