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rs3130783

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs3130783(A;A)
Make rs3130783(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position30806580
is asnp
is mentioned by
dbSNPrs3130783
ebirs3130783
HLIrs3130783
Exacrs3130783
Varsomers3130783
Maprs3130783
PheGenIrs3130783
hapmaprs3130783
1000 genomesrs3130783
hgdprs3130783
ensemblrs3130783
gopubmedrs3130783
geneviewrs3130783
scholarrs3130783
googlers3130783
pharmgkbrs3130783
gwascentralrs3130783
openSNPrs3130783
23andMers3130783
23andMe allrs3130783
SNP Nexus

SNPshotrs3130783
SNPdbers3130783
MSV3drs3130783
GWAS Ctlgrs3130783
GMAF0.2626
Max Magnitude0
? (A;A) (A;G) (G;G) 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 A
P-val 2E-11
Odds Ratio 1.16 [1.11-1.20]


ClinVar
Risk rs3130783(A;A)
Alt rs3130783(A;A)
Reference rs3130783(G;G)
Significance Untested
Disease not provided
Variation info
Gene
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.30774357G>A
CLNSRC
CLNACC RCV000190302.1,