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: rs104893832
rs104893832
2 0.925 0.080 3 13854777 missense variant C/T snv 8.0E-06 0.010 1.000 1 2011 2011
dbSNP: rs104893835
rs104893835
4 0.851 0.120 3 13819120 missense variant G/A snv 0.010 1.000 1 2011 2011