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rs121909267

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121909267(C;G)
Make rs121909267(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position122257288
GeneCASR
is asnp
is mentioned by
dbSNPrs121909267
ebirs121909267
HLIrs121909267
Exacrs121909267
Varsomers121909267
Maprs121909267
PheGenIrs121909267
hapmaprs121909267
1000 genomesrs121909267
hgdprs121909267
ensemblrs121909267
gopubmedrs121909267
geneviewrs121909267
scholarrs121909267
googlers121909267
pharmgkbrs121909267
gwascentralrs121909267
openSNPrs121909267
23andMers121909267
23andMe allrs121909267
SNP Nexus

SNPshotrs121909267
SNPdbers121909267
MSV3drs121909267
GWAS Ctlgrs121909267
Max Magnitude0
OMIM601199
Desc
Variant0035
Relatedalso
ClinVar
Risk rs121909267(G;G)
Alt rs121909267(G;G)
Reference rs121909267(C;C)
Significance Pathogenic
Disease Hypocalcemia
Variation info
Gene CASR
CLNDBN Hypocalcemia, autosomal dominant 1, with bartter syndrome
Reversed 0
HGVS NC_000003.11:g.121976135C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000008849.5,