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rs193922437

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs193922437(A;T)
Make rs193922437(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position122284598
GeneCASR
is asnp
is mentioned by
dbSNPrs193922437
ebirs193922437
HLIrs193922437
Exacrs193922437
Varsomers193922437
Maprs193922437
PheGenIrs193922437
hapmaprs193922437
1000 genomesrs193922437
hgdprs193922437
ensemblrs193922437
gopubmedrs193922437
geneviewrs193922437
scholarrs193922437
googlers193922437
pharmgkbrs193922437
gwascentralrs193922437
openSNPrs193922437
23andMers193922437
23andMe allrs193922437
SNP Nexus

SNPshotrs193922437
SNPdbers193922437
MSV3drs193922437
GWAS Ctlgrs193922437
Max Magnitude0
ClinVar
Risk rs193922437(T;T)
Alt rs193922437(T;T)
Reference rs193922437(A;A)
Significance Probable-Pathogenic
Disease Familial hypocalciuric hypercalcemia
Variation info
Gene CASR
CLNDBN Familial hypocalciuric hypercalcemia
Reversed 0
HGVS NC_000003.11:g.122003445A>T
CLNSRC ClinVar
CLNACC RCV000029445.1,