rs121913671

Orientation

plus

Stabilized

plus

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

Make rs121913671(A;A)

Make rs121913671(A;G)

Reference

GRCh38 38.1/141

Chromosome

7

Position

116783353

Gene

MET

is a	snp
is	mentioned by
dbSNP	rs121913671
dbSNP (classic)	rs121913671
ClinGen	rs121913671
ebi	rs121913671
HLI	rs121913671
Exac	rs121913671
Gnomad	rs121913671
Varsome	rs121913671
LitVar	rs121913671
Map	rs121913671
PheGenI	rs121913671
Biobank	rs121913671
1000 genomes	rs121913671
hgdp	rs121913671
ensembl	rs121913671
geneview	rs121913671
scholar	rs121913671
google	rs121913671
pharmgkb	rs121913671
gwascentral	rs121913671
openSNP	rs121913671
23andMe	rs121913671
SNPshot	rs121913671
SNPdbe	rs121913671
MSV3d	rs121913671
GWAS Ctlg	rs121913671

Merged from

Rs28932777

Max Magnitude

0

OMIM	164860
Desc
Variant	0004
Related	also

ClinVar
Risk	rs121913671(A;A) rs121913671(C;C)
Alt	rs121913671(A;A) rs121913671(C;C)
Reference	Rs121913671(G;G)
Significance	Pathogenic
Disease	Renal cell carcinoma Carcinoma
Variation	info
Gene	MET
CLNDBN	Renal cell carcinoma, papillary, 1 Carcinoma
Reversed	0
HGVS	NC_000007.13:g.116423407G>A; NC_000007.13:g.116423407G>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000014898.25, RCV000420939.1, RCV000437499.1,