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: rs104893813
rs104893813
TGFBR2
1 1.000 0.120 3 30672246 missense variant G/A;C;T snv 8.2E-06; 8.2E-06 0.800 1.000 13 2004 2017