Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs34214527
rs34214527
TNXB
0.925 0.040 6 32046679 intron variant C/T snv 0.11
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs369637
rs369637
TNXB
1.000 0.040 6 32058086 synonymous variant C/T snv 9.1E-02 0.10
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 1 2017 2017
dbSNP: rs369637
rs369637
TNXB
1.000 0.040 6 32058086 synonymous variant C/T snv 9.1E-02 0.10
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		0.700 1.000 1 2017 2017
dbSNP: rs375375234
rs375375234
TNXB
6 32044556 synonymous variant A/T snv
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs41268896
rs41268896
TNXB
1.000 0.120 6 32102292 intron variant G/A snv 0.25
CUI: C0011615
Disease: Dermatitis, Atopic
Dermatitis, Atopic 		0.700 1.000 1 2015 2015
dbSNP: rs41316748
rs41316748
TNXB
6 32051735 intron variant T/C snv 2.4E-02
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs429150
rs429150
TNXB
1.000 6 32107786 intron variant T/C;G snv
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.700 1.000 1 2016 2016
dbSNP: rs6937318
rs6937318
TNXB
1.000 0.040 6 32057055 intron variant T/C snv 0.54
CUI: C0149745
Disease: Oral Ulcer
Oral Ulcer 		0.700 1.000 1 2019 2019
dbSNP: rs8111
rs8111
ATF6B ; TNXB
0.925 0.160 6 32115398 3 prime UTR variant C/T snv 0.26
CUI: C0039263
Disease: Takayasu Arteritis
Takayasu Arteritis 		0.700 1.000 1 2015 2015
dbSNP: rs8111
rs8111
ATF6B ; TNXB
0.925 0.160 6 32115398 3 prime UTR variant C/T snv 0.26
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs8283
rs8283
ATF6B ; TNXB
0.882 0.120 6 32115523 3 prime UTR variant A/G snv 0.25
CUI: C0577608
Disease: C4 complement assay (procedure)
C4 complement assay (procedure) 		0.700 1.000 1 2017 2017
dbSNP: rs9267797
rs9267797
TNXB
6 32062923 intron variant C/A;T snv
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018