Gene: TGFBR1 ×
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: rs111854391
rs111854391
TGFBR1
18 0.716 0.280 9 99138006 stop gained C/A;T snv 4.0E-06 0.700 1.000 7 2006 2015
dbSNP: rs113605875
rs113605875
TGFBR1
3 0.882 0.120 9 99149253 missense variant G/A;C;T snv 0.700 1.000 7 2005 2012
dbSNP: rs111426349
rs111426349
TGFBR1
4 0.882 0.120 9 99149252 missense variant C/A;T snv 4.0E-06 0.700 1.000 6 2006 2016
dbSNP: rs1554700672
rs1554700672
TGFBR1
1 1.000 9 99138065 stop gained G/T snv 0.700 1.000 1 2011 2011
dbSNP: rs387906697
rs387906697
TGFBR1
2 1.000 9 99146594 stop gained C/T snv 0.700 1.000 1 2011 2011
dbSNP: rs886039176
rs886039176
TGFBR1
1 1.000 9 99149250 missense variant T/C;G snv 0.700 1.000 1 2019 2019
dbSNP: rs1057524497
rs1057524497
TGFBR1
1 1.000 9 99138017 stop gained G/A;T snv 0.700 0
dbSNP: rs1060502040
rs1060502040
TGFBR1
1 1.000 9 99132634 stop gained C/T snv 0.700 0
dbSNP: rs1554701881
rs1554701881
TGFBR1
1 1.000 9 99144730 splice acceptor variant A/C;G snv 0.700 0
dbSNP: rs1554702262
rs1554702262
TGFBR1
1 1.000 9 99146610 splice donor variant G/A snv 0.700 0
dbSNP: rs1554702463
rs1554702463
TGFBR1
1 1.000 9 99147701 missense variant G/C snv 0.700 0
dbSNP: rs863223832
rs863223832
TGFBR1
1 1.000 9 99142590 missense variant C/A;T snv 0.700 0