Have questions? Visit https://www.reddit.com/r/SNPedia

rs794729659

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794729659(-;-)
Make rs794729659(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position137232627
GeneSLC34A3
is asnp
is mentioned by
dbSNPrs794729659
ClinGenrs794729659
ebirs794729659
HLIrs794729659
Exacrs794729659
Varsomers794729659
Maprs794729659
PheGenIrs794729659
hapmaprs794729659
1000 genomesrs794729659
hgdprs794729659
ensemblrs794729659
gopubmedrs794729659
geneviewrs794729659
scholarrs794729659
googlers794729659
pharmgkbrs794729659
gwascentralrs794729659
openSNPrs794729659
23andMers794729659
23andMe allrs794729659
SNP Nexus

SNPshotrs794729659
SNPdbers794729659
MSV3drs794729659
GWAS Ctlgrs794729659
Max Magnitude0
ClinVar
Risk rs794729659(-;-)
Alt rs794729659(-;-)
Reference Rs794729659(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.140127079delC
CLNSRC OMIM Allelic Variant
CLNACC RCV000001495.3,