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: rs587777175
rs587777175
TFG
2 0.925 0.080 3 100728759 missense variant C/T snv 4.0E-05 7.0E-06 0.800 1.000 4 2013 2019
dbSNP: rs207482230
rs207482230
TFG
5 0.882 0.080 3 100748182 missense variant C/T snv 4.0E-06 0.700 1.000 5 2012 2017
dbSNP: rs376971794
rs376971794
TFG
2 0.925 0.160 3 100728760 missense variant G/A snv 6.4E-05 3.5E-05 0.700 0