rs41281081

Orientation

plus

Stabilized

plus

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

Make rs41281081(A;A)

Make rs41281081(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

7

Position

116796211

Gene

MET

is a	snp
is	mentioned by
dbSNP	rs41281081
dbSNP (classic)	rs41281081
ClinGen	rs41281081
ebi	rs41281081
HLI	rs41281081
Exac	rs41281081
Gnomad	rs41281081
Varsome	rs41281081
LitVar	rs41281081
Map	rs41281081
PheGenI	rs41281081
Biobank	rs41281081
1000 genomes	rs41281081
hgdp	rs41281081
ensembl	rs41281081
geneview	rs41281081
scholar	rs41281081
google	rs41281081
pharmgkb	rs41281081
gwascentral	rs41281081
openSNP	rs41281081
23andMe	rs41281081
SNPshot	rs41281081
SNPdbe	rs41281081
MSV3d	rs41281081
GWAS Ctlg	rs41281081

Max Magnitude

0

[PMID 26402720] MiRNAs Associated Polymorphisms in the 3'UTR of MET Promote the Risk of Non-Small Cell Lung Cancer

ClinVar
Risk	rs41281081(A;A)
Alt	rs41281081(A;A)
Reference	Rs41281081(G;G)
Significance	Probable-non-pathogenic
Disease	Renal cell carcinoma
Variation	info
Gene	MET
CLNDBN	Renal cell carcinoma, papillary, 1
Reversed	0
HGVS	NC_000007.13:g.116436265G>A
CLNSRC
CLNACC	RCV000304082.1,