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rs121918236

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121918236(A;A)
Make rs121918236(A;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position137233722
GeneSLC34A3
is asnp
is mentioned by
dbSNPrs121918236
ebirs121918236
HLIrs121918236
Exacrs121918236
Varsomers121918236
Maprs121918236
PheGenIrs121918236
hapmaprs121918236
1000 genomesrs121918236
hgdprs121918236
ensemblrs121918236
gopubmedrs121918236
geneviewrs121918236
scholarrs121918236
googlers121918236
pharmgkbrs121918236
gwascentralrs121918236
openSNPrs121918236
23andMers121918236
23andMe allrs121918236
SNP Nexus

SNPshotrs121918236
SNPdbers121918236
MSV3drs121918236
GWAS Ctlgrs121918236
GMAF0.0004591
Max Magnitude0
OMIM609826
Desc
Variant0004
Relatedalso
ClinVar
Risk rs121918236(A;A)
Alt rs121918236(A;A)
Reference rs121918236(G;G)
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.140128174G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000001494.3,