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: rs116298992
rs116298992
TNXB
6 32100718 intron variant C/T snv 1.5E-02
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs204883
rs204883
TNXB
1.000 0.120 6 32064966 missense variant G/A;C snv 0.44
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs3130342
rs3130342
TNXB
1.000 0.080 6 32112369 non coding transcript exon variant A/C;G;T snv
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 1.000 1 2018 2018
dbSNP: rs3134954
rs3134954
TNXB
0.882 0.240 6 32104116 intron variant C/T snv 0.90
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 1.000 1 2018 2018
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: 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: 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: 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: 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
dbSNP: rs1150754
rs1150754
TNXB
0.851 0.200 6 32082981 intron variant C/A;T snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 1 2019 2019
dbSNP: rs13199524
rs13199524
TNXB
0.807 0.240 6 32098988 intron variant C/T snv 8.4E-02
CUI: C0003872
Disease: Arthritis, Psoriatic
Arthritis, Psoriatic 		0.700 1.000 1 2019 2019
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