rs121913669

Orientation

plus

Stabilized

plus

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

Make rs121913669(G;T)

Make rs121913669(T;T)

Reference

GRCh38 38.1/141

Chromosome

7

Position

116782027

Gene

MET

is a	snp
is	mentioned by
dbSNP	rs121913669
dbSNP (classic)	rs121913669
ClinGen	rs121913669
ebi	rs121913669
HLI	rs121913669
Exac	rs121913669
Gnomad	rs121913669
Varsome	rs121913669
LitVar	rs121913669
Map	rs121913669
PheGenI	rs121913669
Biobank	rs121913669
1000 genomes	rs121913669
hgdp	rs121913669
ensembl	rs121913669
geneview	rs121913669
scholar	rs121913669
google	rs121913669
pharmgkb	rs121913669
gwascentral	rs121913669
openSNP	rs121913669
23andMe	rs121913669
SNPshot	rs121913669
SNPdbe	rs121913669
MSV3d	rs121913669
GWAS Ctlg	rs121913669

Merged from

Rs28932775

Max Magnitude

0

OMIM	164860
Desc
Variant	0002
Related	also

ClinVar
Risk	rs121913669(A;A) rs121913669(T;T)
Alt	rs121913669(A;A) rs121913669(T;T)
Reference	Rs121913669(G;G)
Significance	Pathogenic
Disease	Renal cell carcinoma
Variation	info
Gene	MET
CLNDBN	Renal cell carcinoma, papillary, 1
Reversed	0
HGVS	NC_000007.13:g.116422081G>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000014896.25,