rs121913673

Orientation

plus

Stabilized

plus

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

Make rs121913673(C;G)

Make rs121913673(G;G)

Reference

GRCh38 38.1/141

Chromosome

7

Position

116782048

Gene

MET

is a	snp
is	mentioned by
dbSNP	rs121913673
dbSNP (classic)	rs121913673
ClinGen	rs121913673
ebi	rs121913673
HLI	rs121913673
Exac	rs121913673
Gnomad	rs121913673
Varsome	rs121913673
LitVar	rs121913673
Map	rs121913673
PheGenI	rs121913673
Biobank	rs121913673
1000 genomes	rs121913673
hgdp	rs121913673
ensembl	rs121913673
geneview	rs121913673
scholar	rs121913673
google	rs121913673
pharmgkb	rs121913673
gwascentral	rs121913673
openSNP	rs121913673
23andMe	rs121913673
SNPshot	rs121913673
SNPdbe	rs121913673
MSV3d	rs121913673
GWAS Ctlg	rs121913673

Merged from

Rs28932778

Max Magnitude

0

OMIM	164860
Desc
Variant	0006
Related	also

ClinVar
Risk	rs121913673(G;G) rs121913673(T;T)
Alt	rs121913673(G;G) rs121913673(T;T)
Reference	Rs121913673(C;C)
Significance	Pathogenic
Disease	Renal cell carcinoma
Variation	info
Gene	MET
CLNDBN	Renal cell carcinoma, papillary, 1
Reversed	0
HGVS	NC_000007.13:g.116422102C>G; NC_000007.13:g.116422102C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000014900.4, RCV000236718.1,