rs716274

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;A)	0	common in clinvar

Make rs716274(A;G)

Make rs716274(G;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

103547430

is a	snp
is	mentioned by
dbSNP	rs716274
dbSNP (classic)	rs716274
ClinGen	rs716274
ebi	rs716274
HLI	rs716274
Exac	rs716274
Gnomad	rs716274
Varsome	rs716274
LitVar	rs716274
Map	rs716274
PheGenI	rs716274
Biobank	rs716274
1000 genomes	rs716274
hgdp	rs716274
ensembl	rs716274
geneview	rs716274
scholar	rs716274
google	rs716274
pharmgkb	rs716274
gwascentral	rs716274
openSNP	rs716274
23andMe	rs716274
SNPshot	rs716274
SNPdbe	rs716274
MSV3d	rs716274
GWAS Ctlg	rs716274

GMAF

0.4343

Max Magnitude

0

?	(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
CLNACC	RCV000211218.1, RCV000211343.1,