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rs10453441

From SNPedia

Orientationplus
Make rs10453441(A;A)
Make rs10453441(A;G)
Make rs10453441(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome22
Position45967859
GeneWNT7B
is asnp
is mentioned by
dbSNPrs10453441
ebirs10453441
HLIrs10453441
Exacrs10453441
Varsomers10453441
Maprs10453441
PheGenIrs10453441
hapmaprs10453441
1000 genomesrs10453441
hgdprs10453441
ensemblrs10453441
gopubmedrs10453441
geneviewrs10453441
scholarrs10453441
googlers10453441
pharmgkbrs10453441
gwascentralrs10453441
openSNPrs10453441
23andMers10453441
23andMe allrs10453441
SNP Nexus

SNPshotrs10453441
SNPdbers10453441
MSV3drs10453441
GWAS Ctlgrs10453441
Max Magnitude
? (A;A) (A;G) (G;G) 28

[PMID 27655401] Genome-Wide Association Study Identifies WNT7B as a Novel Locus for Central Corneal Thickness in Latinos.