rs577069249

Orientation

plus

Stabilized

plus

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

Make rs577069249(C;C)

Make rs577069249(C;T)

Reference

GRCh38.p7 38.3/150

Chromosome

3

Position

180650140

Gene

CCDC39

is a	snp
is	mentioned by
dbSNP	rs577069249
dbSNP (classic)	rs577069249
ClinGen	rs577069249
ebi	rs577069249
HLI	rs577069249
Exac	rs577069249
Gnomad	rs577069249
Varsome	rs577069249
LitVar	rs577069249
Map	rs577069249
PheGenI	rs577069249
Biobank	rs577069249
1000 genomes	rs577069249
hgdp	rs577069249
ensembl	rs577069249
geneview	rs577069249
scholar	rs577069249
google	rs577069249
pharmgkb	rs577069249
gwascentral	rs577069249
openSNP	rs577069249
23andMe	rs577069249
SNPshot	rs577069249
SNPdbe	rs577069249
MSV3d	rs577069249
GWAS Ctlg	rs577069249

Max Magnitude

0

ClinVar
Risk	rs577069249(C;C)
Alt	rs577069249(C;C)
Reference	Rs577069249(T;T)
Significance	Pathogenic
Disease	Primary ciliary dyskinesia
Variation	info
Gene	CCDC39
CLNDBN	Primary ciliary dyskinesia
Reversed	0
HGVS	NC_000003.11:g.180367928T>C
CLNSRC
CLNACC	RCV000477112.1,