rs587777502

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;-)	0	common in clinvar
(D;D)	0	common genotype
(T;T)	0	common in clinvar

Make rs587777502(-;GGGCT)

Make rs587777502(GGGCT;GGGCT)

Reference

GRCh38 38.1/142

Chromosome

5

Position

55233261

Gene

CCNO

is a	snp
is	mentioned by
dbSNP	rs587777502
dbSNP (classic)	rs587777502
ClinGen	rs587777502
ebi	rs587777502
HLI	rs587777502
Exac	rs587777502
Gnomad	rs587777502
Varsome	rs587777502
LitVar	rs587777502
Map	rs587777502
PheGenI	rs587777502
Biobank	rs587777502
1000 genomes	rs587777502
hgdp	rs587777502
ensembl	rs587777502
geneview	rs587777502
scholar	rs587777502
google	rs587777502
pharmgkb	rs587777502
gwascentral	rs587777502
openSNP	rs587777502
23andMe	rs587777502
SNPshot	rs587777502
SNPdbe	rs587777502
MSV3d	rs587777502
GWAS Ctlg	rs587777502

Max Magnitude

0

ClinVar
Risk	rs587777502(GGGCC;GGGCC) rs587777502(GGGCT;GGGCT)
Alt	rs587777502(GGGCC;GGGCC) rs587777502(GGGCT;GGGCT)
Reference	Rs587777502(-;-)
Significance	Pathogenic
Disease	Ciliary dyskinesia Kartagener syndrome
Variation	info
Gene	CCNO
CLNDBN	Ciliary dyskinesia, primary, 29 Kartagener syndrome
Reversed	0
HGVS	NC_000005.9:g.54529085_54529089dupGGGCT
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000128544.3, RCV000190943.1,