rs1553253989, SLC25A24

N. diseases: 2
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.
Progeroid Syndrome, Congenital, Petty Type
CUI: C2676780
Disease: Progeroid Syndrome, Congenital, Petty Type
2 1.000 0.160 1 108157481 missense variant C/T snv 0.810 1.000 2 2017 2018
Gorlin Chaudhry Moss syndrome
CUI: C0345382
Disease: Gorlin Chaudhry Moss syndrome
2 1.000 0.160 1 108157481 missense variant C/T snv 0.010 1.000 1 2017 2017