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rs8135665

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs8135665(C;T)
Make rs8135665(T;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position38080269
GeneSLC16A8
is asnp
is mentioned by
dbSNPrs8135665
ebirs8135665
HLIrs8135665
Exacrs8135665
Varsomers8135665
Maprs8135665
PheGenIrs8135665
hapmaprs8135665
1000 genomesrs8135665
hgdprs8135665
ensemblrs8135665
gopubmedrs8135665
geneviewrs8135665
scholarrs8135665
googlers8135665
pharmgkbrs8135665
gwascentralrs8135665
openSNPrs8135665
23andMers8135665
23andMe allrs8135665
SNP Nexus

SNPshotrs8135665
SNPdbers8135665
MSV3drs8135665
GWAS Ctlgrs8135665
GMAF0.2236
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23455636OA-icon.png]
Trait Age-related macular degeneration
Title Seven new loci associated with age-related macular degeneration.
Risk Allele T
P-val 2E-11
Odds Ratio 1.15 [1.11-1.19]


ClinVar
Risk rs8135665(T;T)
Alt rs8135665(T;T)
Reference rs8135665(C;C)
Significance Untested
Disease not provided
Variation info
Gene LOC101927119 SLC16A8
CLNDBN not provided
Reversed 0
HGVS NC_000022.10:g.38476276C>T
CLNSRC
CLNACC RCV000190316.1,