rs397515392

Orientation

minus

Stabilized

minus

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

Make rs397515392(C;C)

Make rs397515392(C;G)

Reference

GRCh38 38.1/141

Chromosome

3

Position

180661860

Gene

CCDC39

is a	snp
is	mentioned by
dbSNP	rs397515392
dbSNP (classic)	rs397515392
ClinGen	rs397515392
ebi	rs397515392
HLI	rs397515392
Exac	rs397515392
Gnomad	rs397515392
Varsome	rs397515392
LitVar	rs397515392
Map	rs397515392
PheGenI	rs397515392
Biobank	rs397515392
1000 genomes	rs397515392
hgdp	rs397515392
ensembl	rs397515392
geneview	rs397515392
scholar	rs397515392
google	rs397515392
pharmgkb	rs397515392
gwascentral	rs397515392
openSNP	rs397515392
23andMe	rs397515392
SNPshot	rs397515392
SNPdbe	rs397515392
MSV3d	rs397515392
GWAS Ctlg	rs397515392

Max Magnitude

0

ClinVar
Risk	rs397515392(C;C)
Alt	rs397515392(C;C)
Reference	Rs397515392(G;G)
Significance	Pathogenic
Disease	Ciliary dyskinesia Primary ciliary dyskinesia
Variation	info
Gene	CCDC39
CLNDBN	Ciliary dyskinesia, primary, 14 Primary ciliary dyskinesia
Reversed	1
HGVS	NC_000003.11:g.180379648C>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000024061.3, RCV000199155.3,