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rs193922436

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs193922436(A;A)
Make rs193922436(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position122284443
GeneCASR
is asnp
is mentioned by
dbSNPrs193922436
ebirs193922436
HLIrs193922436
Exacrs193922436
Varsomers193922436
Maprs193922436
PheGenIrs193922436
hapmaprs193922436
1000 genomesrs193922436
hgdprs193922436
ensemblrs193922436
gopubmedrs193922436
geneviewrs193922436
scholarrs193922436
googlers193922436
pharmgkbrs193922436
gwascentralrs193922436
openSNPrs193922436
23andMers193922436
23andMe allrs193922436
SNP Nexus

SNPshotrs193922436
SNPdbers193922436
MSV3drs193922436
GWAS Ctlgrs193922436
Max Magnitude0
ClinVar
Risk rs193922436(A;A)
Alt rs193922436(A;A)
Reference rs193922436(G;G)
Significance Probable-Pathogenic
Disease Familial hypocalciuric hypercalcemia
Variation info
Gene CASR
CLNDBN Familial hypocalciuric hypercalcemia
Reversed 0
HGVS NC_000003.11:g.122003290G>A
CLNSRC ClinVar LabCorp
CLNACC RCV000029444.1,