rs797045150

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(A;A)	0	common in clinvar

Make rs797045150(A;G)

Make rs797045150(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

5

Position

55231712

Gene

CCNO

is a	snp
is	mentioned by
dbSNP	rs797045150
dbSNP (classic)	rs797045150
ClinGen	rs797045150
ebi	rs797045150
HLI	rs797045150
Exac	rs797045150
Gnomad	rs797045150
Varsome	rs797045150
LitVar	rs797045150
Map	rs797045150
PheGenI	rs797045150
Biobank	rs797045150
1000 genomes	rs797045150
hgdp	rs797045150
ensembl	rs797045150
geneview	rs797045150
scholar	rs797045150
google	rs797045150
pharmgkb	rs797045150
gwascentral	rs797045150
openSNP	rs797045150
23andMe	rs797045150
SNPshot	rs797045150
SNPdbe	rs797045150
MSV3d	rs797045150
GWAS Ctlg	rs797045150

Max Magnitude

0

ClinVar
Risk	rs797045150(G;G)
Alt	rs797045150(G;G)
Reference	Rs797045150(A;A)
Significance	Pathogenic
Disease	Kartagener syndrome
Variation	info
Gene	CCNO
CLNDBN	Kartagener syndrome
Reversed	1
HGVS	NC_000005.9:g.54527540T>C
CLNSRC	UniProtKB (protein)
CLNACC	RCV000190945.1,