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rs875989883

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs875989883(A;A)
Make rs875989883(A;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position22219070
GenePHEX, PTCHD1-AS
is asnp
is mentioned by
dbSNPrs875989883
ebirs875989883
HLIrs875989883
Exacrs875989883
Varsomers875989883
Maprs875989883
PheGenIrs875989883
hapmaprs875989883
1000 genomesrs875989883
hgdprs875989883
ensemblrs875989883
gopubmedrs875989883
geneviewrs875989883
scholarrs875989883
googlers875989883
pharmgkbrs875989883
gwascentralrs875989883
openSNPrs875989883
23andMers875989883
23andMe allrs875989883
SNP Nexus

SNPshotrs875989883
SNPdbers875989883
MSV3drs875989883
GWAS Ctlgrs875989883
Max Magnitude0
ClinVar
Risk rs875989883(A;A)
Alt rs875989883(A;A)
Reference rs875989883(G;G)
Significance Probable-Pathogenic
Disease Familial X-linked hypophosphatemic vitamin D refractory rickets
Variation info
Gene PTCHD1-AS PHEX
CLNDBN Familial X-linked hypophosphatemic vitamin D refractory rickets
Reversed 0
HGVS NC_000023.10:g.22237187G>A
CLNSRC University Hospital of Geneva
CLNACC RCV000211521.1,