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rs716274

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs716274(A;G)
Make rs716274(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position103547430
is asnp
is mentioned by
dbSNPrs716274
ebirs716274
HLIrs716274
Exacrs716274
Varsomers716274
Maprs716274
PheGenIrs716274
hapmaprs716274
1000 genomesrs716274
hgdprs716274
ensemblrs716274
gopubmedrs716274
geneviewrs716274
scholarrs716274
googlers716274
pharmgkbrs716274
gwascentralrs716274
openSNPrs716274
23andMers716274
23andMe allrs716274
SNP Nexus

SNPshotrs716274
SNPdbers716274
MSV3drs716274
GWAS Ctlgrs716274
GMAF0.4343
Max Magnitude0
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 21118971]
Trait
Title Genome-Wide Interrogation Identifies YAP1 Variants Associated with Survival of Small-Cell Lung Cancer Patients
Risk Allele G
P-val 9E-8
Odds Ratio 1.8300 [1.47-2.29] (AG)


ClinVar
Risk rs716274(G;G)
Alt rs716274(G;G)
Reference rs716274(A;A)
Significance Drug-response
Disease etoposide response - Toxicity/ADR Platinum compounds response - Toxicity/ADR
Variation info
Gene
CLNDBN etoposide response - Toxicity/ADR Platinum compounds response - Toxicity/ADR
Reversed 0
HGVS NC_000011.9:g.103418158A>G
CLNSRC PharmGKB Clinical Annotation PharmGKB
CLNACC RCV000211218.1, RCV000211343.1,