rs2305089, TBXT

N. diseases: 7
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Chordoma
CUI: C0008487
Disease: Chordoma
3 0.827 0.120 6 166165782 missense variant C/T snv 0.48 0.43 0.050 1.000 5 2012 2017
Asthma
CUI: C0004096
Disease: Asthma
1536 0.827 0.120 6 166165782 missense variant C/T snv 0.48 0.43 0.010 1.000 1 2016 2016
Familial (FPAH)
CUI: C1611743
Disease: Familial (FPAH)
276 0.827 0.120 6 166165782 missense variant C/T snv 0.48 0.43 0.010 1.000 1 2014 2014
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.827 0.120 6 166165782 missense variant C/T snv 0.48 0.43 0.010 1.000 1 2013 2013
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.827 0.120 6 166165782 missense variant C/T snv 0.48 0.43 0.010 1.000 1 2013 2013
Skull Base Chordoma
CUI: C1335975
Disease: Skull Base Chordoma
1 0.827 0.120 6 166165782 missense variant C/T snv 0.48 0.43 0.010 1.000 1 2017 2017
Vertebral chordoma
CUI: C1859101
Disease: Vertebral chordoma
1 0.827 0.120 6 166165782 missense variant C/T snv 0.48 0.43 0.010 1.000 1 2017 2017