Source: ALL
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: rs28934581
rs28934581
TH
1 1.000 0.040 11 2166995 missense variant T/G snv 1.5E-05 0.800 1.000 20 1995 2014