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: rs104893968
rs104893968
8 0.790 0.200 6 42173762 missense variant C/G;T snv 4.0E-06; 1.2E-03 0.020 1.000 2 2001 2001
dbSNP: rs121434631
rs121434631
6 0.807 0.080 6 42179248 missense variant C/G;T snv 4.0E-06 0.010 1.000 1 2013 2013