rs77010315, SLC36A2

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.
HYPERGLYCINURIA (disorder)
CUI: C0543541
Disease: HYPERGLYCINURIA (disorder)
3 0.925 0.160 5 151343594 missense variant C/A snv 9.4E-03 8.6E-03 0.700 0
Iminoglycinuria
CUI: C0268654
Disease: Iminoglycinuria
2 0.925 0.160 5 151343594 missense variant C/A snv 9.4E-03 8.6E-03 0.700 0