Gene: TNXB ×
Source: GWASDB ×
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: rs1150752
rs1150752
TNXB
3 0.882 0.240 6 32096949 missense variant T/C;G snv 5.9E-02 0.700 1.000 1 2007 2007
dbSNP: rs1150754
rs1150754
TNXB
2 0.851 0.200 6 32082981 intron variant C/A;T snv 0.700 1.000 1 2007 2007
dbSNP: rs12153855
rs12153855
TNXB
10 0.776 0.320 6 32107027 intron variant T/C snv 0.11 0.700 1.000 1 2007 2007
dbSNP: rs12198173
rs12198173
TNXB
9 0.827 0.240 6 32059031 intron variant G/A snv 0.10 0.700 1.000 1 2007 2007
dbSNP: rs13199524
rs13199524
TNXB
8 0.807 0.240 6 32098988 intron variant C/T snv 8.4E-02 0.700 1.000 1 2007 2007
dbSNP: rs185819
rs185819
TNXB
8 0.851 0.200 6 32082290 missense variant T/A;C;G snv 8.2E-06; 0.58; 4.1E-06 0.700 1.000 1 2007 2007
dbSNP: rs2269426
rs2269426
TNXB
8 0.807 0.280 6 32108722 intron variant G/A snv 0.35 0.700 1.000 1 2007 2007
dbSNP: rs3134954
rs3134954
TNXB
3 0.882 0.240 6 32104116 intron variant C/T snv 0.90 0.700 1.000 1 2007 2007