rs150547487, SLX4

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 chromosomal disease
CUI: C0008626
Disease: Congenital chromosomal disease
47 16 3597425 missense variant T/C snv 9.9E-04 4.1E-03 0.010 1.000 1 2015 2015