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: rs104893811
rs104893811
TGFBR2
4 0.851 0.160 3 30674228 missense variant C/T snv 0.010 < 0.001 1 2010 2010