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rs77530448

From SNPedia

Orientationplus
Stabilizedplus
Make rs77530448(A;A)
Make rs77530448(A;G)
Make rs77530448(G;G)
ReferenceGRCh38.p7 38.3/149
Chromosome2
Position174729547
is asnp
is mentioned by
dbSNPrs77530448
dbSNP (classic)rs77530448
ClinGenrs77530448
ebirs77530448
HLIrs77530448
Exacrs77530448
Gnomadrs77530448
Varsomers77530448
LitVarrs77530448
Maprs77530448
PheGenIrs77530448
Biobankrs77530448
1000 genomesrs77530448
hgdprs77530448
ensemblrs77530448
geneviewrs77530448
scholarrs77530448
googlers77530448
pharmgkbrs77530448
gwascentralrs77530448
openSNPrs77530448
23andMers77530448
23andMe allrs77530448
SNPshotrs77530448
SNPdbers77530448
MSV3drs77530448
GWAS Ctlgrs77530448
Max Magnitude0
GWAS snp
PMID [PMID 27515689OA-icon.png]
Trait
Title Meta-analysis of Genome Wide Association Studies Identifies Genetic Markers of Late Toxicity Following Radiotherapy for Prostate Cancer.
Risk Allele
P-val
Odds Ratio