AS3MT, arsenite methyltransferase, 57412

N. diseases: 56; N. variants: 18
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs3740393
rs3740393
0.776 0.280 10 102876898 intron variant G/C;T snv
CUI: C0025312
Disease: Meningomyelocele
Meningomyelocele
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases 0.010 1.000 1 2015 2015