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rs193922426

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs193922426(C;C)
Make rs193922426(C;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position122282189
GeneCASR
is asnp
is mentioned by
dbSNPrs193922426
ebirs193922426
HLIrs193922426
Exacrs193922426
Varsomers193922426
Maprs193922426
PheGenIrs193922426
hapmaprs193922426
1000 genomesrs193922426
hgdprs193922426
ensemblrs193922426
gopubmedrs193922426
geneviewrs193922426
scholarrs193922426
googlers193922426
pharmgkbrs193922426
gwascentralrs193922426
openSNPrs193922426
23andMers193922426
23andMe allrs193922426
SNP Nexus

SNPshotrs193922426
SNPdbers193922426
MSV3drs193922426
GWAS Ctlgrs193922426
Max Magnitude0
ClinVar
Risk rs193922426(C;C)
Alt rs193922426(C;C)
Reference rs193922426(G;G)
Significance Probable-Pathogenic
Disease Familial hypocalciuric hypercalcemia
Variation info
Gene CASR
CLNDBN Familial hypocalciuric hypercalcemia
Reversed 0
HGVS NC_000003.11:g.122001036G>C
CLNSRC ClinVar LabCorp
CLNACC RCV000029433.1,