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rs205611

From SNPedia

Orientationplus
Stabilizedplus
Make rs205611(A;A)
Make rs205611(A;G)
Make rs205611(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position74744954
GeneLOC102724497
is asnp
is mentioned by
dbSNPrs205611
ebirs205611
HLIrs205611
Exacrs205611
Varsomers205611
Maprs205611
PheGenIrs205611
hapmaprs205611
1000 genomesrs205611
hgdprs205611
ensemblrs205611
gopubmedrs205611
geneviewrs205611
scholarrs205611
googlers205611
pharmgkbrs205611
gwascentralrs205611
openSNPrs205611
23andMers205611
23andMe allrs205611
SNP Nexus

SNPshotrs205611
SNPdbers205611
MSV3drs205611
GWAS Ctlgrs205611
GMAF0.09504
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 21835309OA-icon.png]
Trait
Title GWAS findings for human iris patterns: associations with variants in genes that influence normal neuronal pattern development.
Risk Allele A
P-val 0.000001
Odds Ratio 0.1200 [0.06-0.18] unit decrease