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: rs207482230
rs207482230
TFG
5 0.882 0.080 3 100748182 missense variant C/T snv 4.0E-06 0.010 1.000 1 2017 2017