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rs875989883

From SNPedia

ClinVar
Risk rs875989883(A;A)
Alt rs875989883(A;A)
Reference Rs875989883(G;G)
Significance Pathogenic
Disease Familial X-linked hypophosphatemic vitamin D refractory rickets not provided
Variation info
Gene PTCHD1-AS PHEX
CLNDBN Familial X-linked hypophosphatemic vitamin D refractory rickets not provided
Reversed 0
HGVS NC_000023.10:g.22237187G>A
CLNSRC University Hospital of Geneva
CLNACC RCV000211521.1, RCV000396672.2,