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rs193922419

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs193922419(A;C)
Make rs193922419(C;C)
ReferenceGRCh38 38.1/141
Chromosome3
Position122262093
GeneCASR
is asnp
is mentioned by
dbSNPrs193922419
ebirs193922419
HLIrs193922419
Exacrs193922419
Varsomers193922419
Maprs193922419
PheGenIrs193922419
hapmaprs193922419
1000 genomesrs193922419
hgdprs193922419
ensemblrs193922419
gopubmedrs193922419
geneviewrs193922419
scholarrs193922419
googlers193922419
pharmgkbrs193922419
gwascentralrs193922419
openSNPrs193922419
23andMers193922419
23andMe allrs193922419
SNP Nexus

SNPshotrs193922419
SNPdbers193922419
MSV3drs193922419
GWAS Ctlgrs193922419
Max Magnitude0
ClinVar
Risk rs193922419(C;C)
Alt rs193922419(C;C)
Reference rs193922419(A;A)
Significance Probable-Pathogenic
Disease Familial hypocalciuric hypercalcemia
Variation info
Gene CASR
CLNDBN Familial hypocalciuric hypercalcemia
Reversed 0
HGVS NC_000003.11:g.121980940A>C
CLNSRC ClinVar LabCorp
CLNACC RCV000029425.1,