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rs4902566

From SNPedia

Orientationplus
Stabilizedplus
Make rs4902566(C;C)
Make rs4902566(C;T)
Make rs4902566(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position68326837
GeneRAD51B
is asnp
is mentioned by
dbSNPrs4902566
ebirs4902566
HLIrs4902566
Exacrs4902566
Varsomers4902566
Maprs4902566
PheGenIrs4902566
hapmaprs4902566
1000 genomesrs4902566
hgdprs4902566
ensemblrs4902566
gopubmedrs4902566
geneviewrs4902566
scholarrs4902566
googlers4902566
pharmgkbrs4902566
gwascentralrs4902566
openSNPrs4902566
23andMers4902566
23andMe allrs4902566
SNP Nexus

SNPshotrs4902566
SNPdbers4902566
MSV3drs4902566
GWAS Ctlgrs4902566
GMAF0.3958
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 24526414OA-icon.png] In-depth analyses unveil the association and possible functional involvement of novel RAD51B polymorphisms in age-related macular degeneration