rs587777779

Orientation

plus

Stabilized

plus

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

Make rs587777779(A;A)

Make rs587777779(A;C)

Reference

GRCh38 38.1/142

Chromosome

19

Position

11426182

Gene

CCDC151

is a	snp
is	mentioned by
dbSNP	rs587777779
dbSNP (classic)	rs587777779
ClinGen	rs587777779
ebi	rs587777779
HLI	rs587777779
Exac	rs587777779
Gnomad	rs587777779
Varsome	rs587777779
LitVar	rs587777779
Map	rs587777779
PheGenI	rs587777779
Biobank	rs587777779
1000 genomes	rs587777779
hgdp	rs587777779
ensembl	rs587777779
geneview	rs587777779
scholar	rs587777779
google	rs587777779
pharmgkb	rs587777779
gwascentral	rs587777779
openSNP	rs587777779
23andMe	rs587777779
SNPshot	rs587777779
SNPdbe	rs587777779
MSV3d	rs587777779
GWAS Ctlg	rs587777779

Max Magnitude

0

ClinVar
Risk	rs587777779(A;A)
Alt	rs587777779(A;A)
Reference	Rs587777779(C;C)
Significance	Pathogenic
Disease	Ciliary dyskinesia Kartagener syndrome
Variation	info
Gene	CCDC151
CLNDBN	Ciliary dyskinesia, primary, 30 Kartagener syndrome
Reversed	0
HGVS	NC_000019.9:g.11537002C>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000144449.3, RCV000190932.1,