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rs794729658

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794729658(-;-)
Make rs794729658(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position137233924
GeneSLC34A3
is asnp
is mentioned by
dbSNPrs794729658
dbSNP (old)rs794729658
ClinGenrs794729658
ebirs794729658
HLIrs794729658
Exacrs794729658
Gnomadrs794729658
Varsomers794729658
Maprs794729658
PheGenIrs794729658
Biobankrs794729658
1000 genomesrs794729658
hgdprs794729658
ensemblrs794729658
gopubmedrs794729658
geneviewrs794729658
scholarrs794729658
googlers794729658
pharmgkbrs794729658
gwascentralrs794729658
openSNPrs794729658
23andMers794729658
23andMe allrs794729658
SNP Nexus

SNPshotrs794729658
SNPdbers794729658
MSV3drs794729658
GWAS Ctlgrs794729658
Max Magnitude0
ClinVar
Risk rs794729658(-;-)
Alt rs794729658(-;-)
Reference Rs794729658(C;C)
Significance Pathogenic
Disease Autosomal recessive hypophosphatemic bone disease
Variation info
Gene SLC34A3
CLNDBN Autosomal recessive hypophosphatemic bone disease
Reversed 0
HGVS NC_000009.11:g.140128376delC
CLNSRC OMIM Allelic Variant
CLNACC RCV000001491.3,