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rs121909261

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121909261(G;T)
Make rs121909261(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position122283997
GeneCASR
is asnp
is mentioned by
dbSNPrs121909261
ebirs121909261
HLIrs121909261
Exacrs121909261
Varsomers121909261
Maprs121909261
PheGenIrs121909261
hapmaprs121909261
1000 genomesrs121909261
hgdprs121909261
ensemblrs121909261
gopubmedrs121909261
geneviewrs121909261
scholarrs121909261
googlers121909261
pharmgkbrs121909261
gwascentralrs121909261
openSNPrs121909261
23andMers121909261
23andMe allrs121909261
SNP Nexus

SNPshotrs121909261
SNPdbers121909261
MSV3drs121909261
GWAS Ctlgrs121909261
Max Magnitude0
OMIM601199
Desc
Variant0009
Relatedalso
ClinVar
Risk rs121909261(T;T)
Alt rs121909261(T;T)
Reference rs121909261(G;G)
Significance Pathogenic
Disease Hypocalcemia
Variation info
Gene CASR
CLNDBN Hypocalcemia, autosomal dominant 1
Reversed 0
HGVS NC_000003.11:g.122002844G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000008821.3,