rs4937076

Orientation

plus

Stabilized

plus

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

Make rs4937076(A;A)

Make rs4937076(A;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

125956807

Gene	CDON, LOC338667

is a	snp
is	mentioned by
dbSNP	rs4937076
dbSNP (classic)	rs4937076
ClinGen	rs4937076
ebi	rs4937076
HLI	rs4937076
Exac	rs4937076
Gnomad	rs4937076
Varsome	rs4937076
LitVar	rs4937076
Map	rs4937076
PheGenI	rs4937076
Biobank	rs4937076
1000 genomes	rs4937076
hgdp	rs4937076
ensembl	rs4937076
geneview	rs4937076
scholar	rs4937076
google	rs4937076
pharmgkb	rs4937076
gwascentral	rs4937076
openSNP	rs4937076
23andMe	rs4937076
SNPshot	rs4937076
SNPdbe	rs4937076
MSV3d	rs4937076
GWAS Ctlg	rs4937076

GMAF

0.4972

Max Magnitude

0

?	(A;A) (A;G) (G;G)	28

GWAS snp
PMID	[PMID 23704328]
Trait	Primary tooth development (time to first tooth eruption)
Title	Genome-wide association study of primary tooth eruption identifies pleiotropic loci associated with height and craniofacial distances.
Risk Allele	A
P-val	4E-8
Odds Ratio	.15 [0.097-0.203] unit decrease

ClinVar
Risk	rs4937076(A;A)
Alt	rs4937076(A;A)
Reference	Rs4937076(G;G)
Significance	Non-pathogenic
Disease	Holoprosencephaly
Variation	info
Gene	LOC338667 CDON
CLNDBN	Holoprosencephaly
Reversed	0
HGVS	NC_000011.9:g.125826702G>A
CLNSRC
CLNACC	RCV000383985.1,