rs4373767

Orientation

plus

Stabilized

plus

Make rs4373767(C;C)

Make rs4373767(C;T)

Make rs4373767(T;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

219586340

is a	snp
is	mentioned by
dbSNP	rs4373767
dbSNP (classic)	rs4373767
ClinGen	rs4373767
ebi	rs4373767
HLI	rs4373767
Exac	rs4373767
Gnomad	rs4373767
Varsome	rs4373767
LitVar	rs4373767
Map	rs4373767
PheGenI	rs4373767
Biobank	rs4373767
1000 genomes	rs4373767
hgdp	rs4373767
ensembl	rs4373767
geneview	rs4373767
scholar	rs4373767
google	rs4373767
pharmgkb	rs4373767
gwascentral	rs4373767
openSNP	rs4373767
23andMe	rs4373767
SNPshot	rs4373767
SNPdbe	rs4373767
MSV3d	rs4373767
GWAS Ctlg	rs4373767

GMAF

0.3636

Max Magnitude

0

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

GWAS snp
PMID	[PMID 22685421]
Trait
Title	Genetic variants on chromosome 1q41 influence ocular axial length and high myopia.
Risk Allele	C
P-val	3E-10
Odds Ratio	0.1600 None

[PMID 31300455] Association of the ZC3H11B, ZFHX1B and SNTB1 genes with myopia of different severities.

[PMID 32816751] Genetic associations of myopia severities and endophenotypes in children.