rs76322625

Orientation

plus

Stabilized

plus

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

Make rs76322625(C;T)

Make rs76322625(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

7

Position

116798111

Gene

MET

is a	snp
is	mentioned by
dbSNP	rs76322625
dbSNP (classic)	rs76322625
ClinGen	rs76322625
ebi	rs76322625
HLI	rs76322625
Exac	rs76322625
Gnomad	rs76322625
Varsome	rs76322625
LitVar	rs76322625
Map	rs76322625
PheGenI	rs76322625
Biobank	rs76322625
1000 genomes	rs76322625
hgdp	rs76322625
ensembl	rs76322625
geneview	rs76322625
scholar	rs76322625
google	rs76322625
pharmgkb	rs76322625
gwascentral	rs76322625
openSNP	rs76322625
23andMe	rs76322625
SNPshot	rs76322625
SNPdbe	rs76322625
MSV3d	rs76322625
GWAS Ctlg	rs76322625

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	rs76322625(A;A) rs76322625(T;T)
Alt	rs76322625(A;A) rs76322625(T;T)
Reference	Rs76322625(C;C)
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.116438165C>T
CLNSRC
CLNACC	RCV000272297.1,