rs1211950654, CYP26B1

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.
Congenital abnormal Synostosis
CUI: C0039093
Disease: Congenital abnormal Synostosis
7 1.000 0.080 2 72132463 missense variant C/T snv 4.0E-06 0.010 1.000 1 2016 2016