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rs193922701

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs193922701(C;C)
Make rs193922701(C;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position4379421
GeneFGF23
is asnp
is mentioned by
dbSNPrs193922701
ebirs193922701
HLIrs193922701
Exacrs193922701
Varsomers193922701
Maprs193922701
PheGenIrs193922701
hapmaprs193922701
1000 genomesrs193922701
hgdprs193922701
ensemblrs193922701
gopubmedrs193922701
geneviewrs193922701
scholarrs193922701
googlers193922701
pharmgkbrs193922701
gwascentralrs193922701
openSNPrs193922701
23andMers193922701
23andMe allrs193922701
SNP Nexus

SNPshotrs193922701
SNPdbers193922701
MSV3drs193922701
GWAS Ctlgrs193922701
Max Magnitude0
ClinVar
Risk rs193922701(C;C)
Alt rs193922701(C;C)
Reference rs193922701(G;G)
Significance Probable-Pathogenic
Disease Autosomal dominant hypophosphatemic rickets
Variation info
Gene FGF23
CLNDBN Autosomal dominant hypophosphatemic rickets
Reversed 1
HGVS NC_000012.11:g.4488587C>G
CLNSRC ClinVar LabCorp
CLNACC RCV000029797.1,