rs2293485, STX1A

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.
Facial Hemiatrophy
CUI: C0015458
Disease: Facial Hemiatrophy
4 1.000 0.080 7 73708593 synonymous variant A/G snv 0.010 1.000 1 2008 2008