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rs1960445

From SNPedia

Orientationplus
Stabilizedplus
Make rs1960445(C;C)
Make rs1960445(C;T)
Make rs1960445(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position81009660
is asnp
is mentioned by
dbSNPrs1960445
ebirs1960445
HLIrs1960445
Exacrs1960445
Varsomers1960445
Maprs1960445
PheGenIrs1960445
hapmaprs1960445
1000 genomesrs1960445
hgdprs1960445
ensemblrs1960445
gopubmedrs1960445
geneviewrs1960445
scholarrs1960445
googlers1960445
pharmgkbrs1960445
gwascentralrs1960445
openSNPrs1960445
23andMers1960445
23andMe allrs1960445
SNP Nexus

SNPshotrs1960445
SNPdbers1960445
MSV3drs1960445
GWAS Ctlgrs1960445
GMAF0.1671
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23396134OA-icon.png]
Trait Refractive error
Title Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia.
Risk Allele C
P-val 1E-6
Odds Ratio .11 [0.067-0.161] unit decrease