rs104893833

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(G;G)	0	common in complete genomics

Make rs104893833(C;C)

Make rs104893833(C;G)

Reference

GRCh38 38.1/141

Chromosome

4

Position

26490207

Gene

CCKAR

is a	snp
is	mentioned by
dbSNP	rs104893833
dbSNP (classic)	rs104893833
ClinGen	rs104893833
ebi	rs104893833
HLI	rs104893833
Exac	rs104893833
Gnomad	rs104893833
Varsome	rs104893833
LitVar	rs104893833
Map	rs104893833
PheGenI	rs104893833
Biobank	rs104893833
1000 genomes	rs104893833
hgdp	rs104893833
ensembl	rs104893833
geneview	rs104893833
scholar	rs104893833
google	rs104893833
pharmgkb	rs104893833
gwascentral	rs104893833
openSNP	rs104893833
23andMe	rs104893833
SNPshot	rs104893833
SNPdbe	rs104893833
MSV3d	rs104893833
GWAS Ctlg	rs104893833

GMAF

0.0004591

Max Magnitude

0

OMIM	118444
Desc
Variant	0001
Related	also

ClinVar
Risk	rs104893833(A;A) rs104893833(C;C)
Alt	rs104893833(A;A) rs104893833(C;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,