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rs8017304

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs8017304(A;A)
Make rs8017304(A;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position68318360
GeneRAD51B
is asnp
is mentioned by
dbSNPrs8017304
ebirs8017304
HLIrs8017304
Exacrs8017304
Varsomers8017304
Maprs8017304
PheGenIrs8017304
hapmaprs8017304
1000 genomesrs8017304
hgdprs8017304
ensemblrs8017304
gopubmedrs8017304
geneviewrs8017304
scholarrs8017304
googlers8017304
pharmgkbrs8017304
gwascentralrs8017304
openSNPrs8017304
23andMers8017304
23andMe allrs8017304
SNP Nexus

SNPshotrs8017304
SNPdbers8017304
MSV3drs8017304
GWAS Ctlgrs8017304
GMAF0.478
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 9E-11
Odds Ratio 1.11 [1.08-1.14]


[PMID 24526414OA-icon.png] In-depth analyses unveil the association and possible functional involvement of novel RAD51B polymorphisms in age-related macular degeneration


ClinVar
Risk rs8017304(A;A)
Alt rs8017304(A;A)
Reference rs8017304(G;G)
Significance Untested
Disease not provided
Variation info
Gene RAD51B
CLNDBN not provided
Reversed 0
HGVS NC_000014.8:g.68785077G>A
CLNSRC
CLNACC RCV000190311.1,