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: rs1481318368
rs1481318368
TH
10 0.827 0.120 11 2169802 missense variant C/T snv 0.010 1.000 1 2003 2003
dbSNP: rs75183227
rs75183227
TH
3 0.882 0.080 11 2169790 missense variant C/A snv 0.010 1.000 1 2017 2017