Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2021783
TNXB
6 32077074 intron variant C/T snv 1.0E-02 3
rs2856451
TNXB
6 32043581 intron variant A/G;T snv 0.59 3
rs8111
ATF6B ; TNXB
0.925 0.160 6 32115398 3 prime UTR variant C/T snv 0.26 2
rs185819
TNXB
0.851 0.200 6 32082290 missense variant T/A;C;G snv 8.2E-06; 0.58; 4.1E-06 2
rs369637
TNXB
1.000 0.040 6 32058086 synonymous variant C/T snv 9.1E-02 0.10 2
rs12153855
TNXB
0.776 0.320 6 32107027 intron variant T/C snv 0.11 2
rs1150757
TNXB
0.925 0.160 6 32061428 synonymous variant G/A;C snv 5.9E-02 2
rs1150754
TNXB
0.851 0.200 6 32082981 intron variant C/A;T snv 2
rs144433536
TNXB
0.925 0.080 6 32067917 synonymous variant C/A;G;T snv 2
rs8283
ATF6B ; TNXB
0.882 0.120 6 32115523 3 prime UTR variant A/G snv 0.25 1
rs13199524
TNXB
0.807 0.240 6 32098988 intron variant C/T snv 8.4E-02 1
rs17207986
TNXB
1.000 0.040 6 32111790 non coding transcript exon variant T/C;G snv 1
rs41268896
TNXB
1.000 0.120 6 32102292 intron variant G/A snv 0.25 1
rs1150755
TNXB
1.000 0.080 6 32070773 intron variant C/T snv 0.10 1
rs1150753
TNXB
0.925 0.120 6 32092090 intron variant A/G snv 6.3E-02 1
rs3130342
TNXB
1.000 0.080 6 32112369 non coding transcript exon variant A/C;G;T snv 1
rs3134954
TNXB
0.882 0.240 6 32104116 intron variant C/T snv 0.90 1
rs6937318
TNXB
1.000 0.040 6 32057055 intron variant T/C snv 0.54 1
rs429150
TNXB
1.000 6 32107786 intron variant T/C;G snv 1
rs2857009
TNXB
1.000 0.080 6 32051969 intron variant G/C snv 0.25 1
rs34214527
TNXB
0.925 0.040 6 32046679 intron variant C/T snv 0.11 1
rs204883
TNXB
1.000 0.120 6 32064966 missense variant G/A;C snv 0.44 1
rs116298992
TNXB
6 32100718 intron variant C/T snv 1.5E-02 1
rs9267797
TNXB
6 32062923 intron variant C/A;T snv 1
rs41316748
TNXB
6 32051735 intron variant T/C snv 2.4E-02 1