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rs3786800

From SNPedia

Orientationminus
Stabilizedminus
Make rs3786800(A;A)
Make rs3786800(A;G)
Make rs3786800(G;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position30499793
GeneZNF536
is asnp
is mentioned by
dbSNPrs3786800
ebirs3786800
HLIrs3786800
Exacrs3786800
Varsomers3786800
Maprs3786800
PheGenIrs3786800
hapmaprs3786800
1000 genomesrs3786800
hgdprs3786800
ensemblrs3786800
gopubmedrs3786800
geneviewrs3786800
scholarrs3786800
googlers3786800
pharmgkbrs3786800
gwascentralrs3786800
openSNPrs3786800
23andMers3786800
23andMe allrs3786800
SNP Nexus

SNPshotrs3786800
SNPdbers3786800
MSV3drs3786800
GWAS Ctlgrs3786800
GMAF0.1791
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 23049088]
Trait Myopia (pathological)
Title A Genome-Wide Association Study Provides Evidence for Association of Chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with High Myopia in the French Population.
Risk Allele
P-val 3E-12
Odds Ratio NR NR