rs104893833

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs104893833(C;C)
Make rs104893833(C;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position26490207
GeneCCKAR
is asnp
is mentioned by
dbSNPrs104893833
ebirs104893833
HLIrs104893833
Exacrs104893833
Varsomers104893833
Maprs104893833
PheGenIrs104893833
hapmaprs104893833
1000 genomesrs104893833
hgdprs104893833
ensemblrs104893833
gopubmedrs104893833
geneviewrs104893833
scholarrs104893833
googlers104893833
pharmgkbrs104893833
gwascentralrs104893833
openSNPrs104893833
23andMers104893833
23andMe allrs104893833
SNP Nexus

SNPshotrs104893833
SNPdbers104893833
MSV3drs104893833
GWAS Ctlgrs104893833
GMAF0.0004591
Max Magnitude0
OMIM118444
Desc
Variant0001
Relatedalso
ClinVar
Risk rs104893833(A,C;A,C)
Alt rs104893833(A,C;A,C)
Reference rs104893833(G;G)
Significance Non-pathogenic
Disease CHOLECYSTOKININ A RECEPTOR POLYMORPHISM
Variation info
Gene CCKAR
CLNDBN CHOLECYSTOKININ A RECEPTOR POLYMORPHISM
Reversed 1
HGVS NC_000004.11:g.26491829C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000019081.2,