Have questions? Visit https://www.reddit.com/r/SNPedia

rs9542236

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs9542236(C;C)
Make rs9542236(C;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position31245188
GeneB3GALTL
is asnp
is mentioned by
dbSNPrs9542236
ebirs9542236
HLIrs9542236
Exacrs9542236
Varsomers9542236
Maprs9542236
PheGenIrs9542236
hapmaprs9542236
1000 genomesrs9542236
hgdprs9542236
ensemblrs9542236
gopubmedrs9542236
geneviewrs9542236
scholarrs9542236
googlers9542236
pharmgkbrs9542236
gwascentralrs9542236
openSNPrs9542236
23andMers9542236
23andMe allrs9542236
SNP Nexus

SNPshotrs9542236
SNPdbers9542236
MSV3drs9542236
GWAS Ctlgrs9542236
GMAF0.2429
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 C
P-val 2E-8
Odds Ratio 1.10 [1.07-1.14]

[PMID 23868022] RAD51 gene is associated with advanced age-related macular degeneration in Chinese population

ClinVar
Risk rs9542236(C;C)
Alt rs9542236(C;C)
Reference rs9542236(T;T)
Significance Untested
Disease not provided
Variation info
Gene B3GLCT
CLNDBN not provided
Reversed 0
HGVS NC_000013.10:g.31819325T>C
CLNSRC
CLNACC RCV000190310.1,