Gene: TNXB ×
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: rs12153855
rs12153855
TNXB
11 0.776 0.320 6 32107027 intron variant T/C snv 0.11 0.700 1.000 2 2009 2010
dbSNP: rs13199524
rs13199524
TNXB
9 0.807 0.240 6 32098988 intron variant C/T snv 8.4E-02 0.700 1.000 2 2009 2010
dbSNP: rs12198173
rs12198173
TNXB
9 0.827 0.240 6 32059031 intron variant G/A snv 0.10 0.700 1.000 1 2010 2010
dbSNP: rs12211410
rs12211410
TNXB
5 0.925 0.120 6 32081646 missense variant C/G;T snv 5.6E-05; 7.7E-02; 3.7E-05 0.700 1.000 1 2010 2010
dbSNP: rs185819
rs185819
TNXB
10 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 2010 2010
dbSNP: rs2269426
rs2269426
TNXB
10 0.807 0.280 6 32108722 intron variant G/A snv 0.35 0.700 1.000 1 2010 2010
dbSNP: rs2856448
rs2856448
TNXB
4 1.000 6 32046798 intron variant A/G snv 0.52 0.700 1.000 1 2010 2010
dbSNP: rs28732175
rs28732175
ATF6B ; TNXB
4 1.000 6 32117501 intron variant C/T snv 2.4E-02 0.700 1.000 1 2010 2010
dbSNP: rs34214527
rs34214527
TNXB
6 0.925 0.040 6 32046679 intron variant C/T snv 0.11 0.700 1.000 1 2010 2010
dbSNP: rs429150
rs429150
TNXB
6 1.000 6 32107786 intron variant T/C;G snv 0.700 1.000 1 2010 2010
dbSNP: rs8283
rs8283
ATF6B ; TNXB
7 0.882 0.120 6 32115523 3 prime UTR variant A/G snv 0.25 0.700 1.000 1 2010 2010