rs1884302

Orientation

plus

Stabilized

plus

Make rs1884302(C;C)

Make rs1884302(C;T)

Make rs1884302(T;T)

Reference

GRCh38 38.1/141

Chromosome

20

Position

7125642

is a	snp
is	mentioned by
dbSNP	rs1884302
dbSNP (classic)	rs1884302
ClinGen	rs1884302
ebi	rs1884302
HLI	rs1884302
Exac	rs1884302
Gnomad	rs1884302
Varsome	rs1884302
LitVar	rs1884302
Map	rs1884302
PheGenI	rs1884302
Biobank	rs1884302
1000 genomes	rs1884302
hgdp	rs1884302
ensembl	rs1884302
geneview	rs1884302
scholar	rs1884302
google	rs1884302
pharmgkb	rs1884302
gwascentral	rs1884302
openSNP	rs1884302
23andMe	rs1884302
SNPshot	rs1884302
SNPdbe	rs1884302
MSV3d	rs1884302
GWAS Ctlg	rs1884302

GMAF

0.4302

Max Magnitude

0

?	(C;C) (C;T) (T;T)	28

GWAS snp
PMID	[PMID 23160099]
Trait	Sagittal craniosynostosis
Title	A genome-wide association study identifies susceptibility loci for nonsyndromic sagittal craniosynostosis near BMP2 and within BBS9.
Risk Allele	C
P-val	1E-39
Odds Ratio	4.38 [3.51-5.45]

ClinVar
Risk	rs1884302(C;C)
Alt	rs1884302(C;C)
Reference	rs1884302(T;T)
Significance	Other
Disease	Craniosynostosis 7
Variation	info
Gene
CLNDBN	Craniosynostosis 7
Reversed	0
HGVS	NC_000020.10:g.7106289T>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000490626.1,