rs1538101, BNC2

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 9 16710872 intron variant A/G snv 0.90 0.700 1.000 1 2018 2018