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: rs104894580
rs104894580
7 0.790 0.240 17 70175238 missense variant C/A;T snv 4.0E-06 0.010 1.000 1 2002 2002
dbSNP: rs104894584
rs104894584
5 0.851 0.120 17 70175553 missense variant G/A snv 0.010 1.000 1 2012 2012