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: rs121909212
rs121909212
TGFBI
6 0.807 0.160 5 136055770 missense variant C/A;G;T snv 3.2E-04; 3.2E-05; 3.6E-05 0.830 0.800 5 1998 2011
dbSNP: rs121909214
rs121909214
TGFBI
1 1.000 0.080 5 136056736 missense variant T/C snv 0.800 1.000 2 1998 2005
dbSNP: rs121909208
rs121909208
TGFBI
13 0.724 0.240 5 136056780 missense variant C/T snv 7.0E-06 0.010 1.000 1 2011 2011
dbSNP: rs121909210
rs121909210
TGFBI
15 0.708 0.200 5 136046406 missense variant C/A;T snv 4.0E-06; 4.0E-06 0.010 1.000 1 2011 2011
dbSNP: rs121909211
rs121909211
TGFBI
15 0.724 0.200 5 136046407 missense variant G/A;T snv 4.0E-05 0.010 1.000 1 2011 2011
dbSNP: rs267607109
rs267607109
TGFBI
5 0.827 0.160 5 136056754 missense variant C/A snv 0.010 1.000 1 2011 2011