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

rs52795588

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs52795588(A;A)
Make rs52795588(A;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position26481832
GeneCCKAR
is asnp
is mentioned by
dbSNPrs52795588
dbSNP (classic)rs52795588
ClinGenrs52795588
ebirs52795588
HLIrs52795588
Exacrs52795588
Gnomadrs52795588
Varsomers52795588
LitVarrs52795588
Maprs52795588
PheGenIrs52795588
Biobankrs52795588
1000 genomesrs52795588
hgdprs52795588
ensemblrs52795588
geneviewrs52795588
scholarrs52795588
googlers52795588
pharmgkbrs52795588
gwascentralrs52795588
openSNPrs52795588
23andMers52795588
SNPshotrs52795588
SNPdbers52795588
MSV3drs52795588
GWAS Ctlgrs52795588
GMAF0.00551
Max Magnitude0
OMIM118444
Desc
Variant0002
Relatedalso


ClinVar
Risk rs52795588(A;A)
Alt rs52795588(A;A)
Reference Rs52795588(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.26483454C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000019082.2,