Have questions? Visit https://www.reddit.com/r/SNPedia

rs140022350

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs140022350(A;G)
Make rs140022350(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position122284359
GeneCASR
is asnp
is mentioned by
dbSNPrs140022350
dbSNP (classic)rs140022350
ClinGenrs140022350
ebirs140022350
HLIrs140022350
Exacrs140022350
Gnomadrs140022350
Varsomers140022350
LitVarrs140022350
Maprs140022350
PheGenIrs140022350
Biobankrs140022350
1000 genomesrs140022350
hgdprs140022350
ensemblrs140022350
geneviewrs140022350
scholarrs140022350
googlers140022350
pharmgkbrs140022350
gwascentralrs140022350
openSNPrs140022350
23andMers140022350
23andMe allrs140022350
SNPshotrs140022350
SNPdbers140022350
MSV3drs140022350
GWAS Ctlgrs140022350
Max Magnitude0
ClinVar
Risk rs140022350(G;G)
Alt rs140022350(G;G)
Reference Rs140022350(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene CASR
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.122003206A>G
CLNSRC
CLNACC RCV000433842.1,