rs145942932, TEKT5

N. diseases: 1
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.
Velopharyngeal dysfunction
CUI: C4280669
Disease: Velopharyngeal dysfunction
33 16 10652766 intron variant ACACACACACACACACAC/-;AC;ACACAC;ACACACAC;ACACACACAC;ACACACACACAC;ACACACACACACAC;ACACACACACACACAC;ACACACACACACACACACAC;ACACACACACACACACACACAC delins 0.52 0.700 1.000 1 2018 2018