rs121913668

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;T)	5.7	Familial papillary renal cell carcinoma
(T;T)	0	common in clinvar

Make rs121913668(C;C)

Reference

GRCh38 38.1/141

Chromosome

7

Position

116778827

Gene

MET

is a	snp
is	mentioned by
dbSNP	rs121913668
dbSNP (classic)	rs121913668
ClinGen	rs121913668
ebi	rs121913668
HLI	rs121913668
Exac	rs121913668
Gnomad	rs121913668
Varsome	rs121913668
LitVar	rs121913668
Map	rs121913668
PheGenI	rs121913668
Biobank	rs121913668
1000 genomes	rs121913668
hgdp	rs121913668
ensembl	rs121913668
geneview	rs121913668
scholar	rs121913668
google	rs121913668
pharmgkb	rs121913668
gwascentral	rs121913668
openSNP	rs121913668
23andMe	rs121913668
SNPshot	rs121913668
SNPdbe	rs121913668
MSV3d	rs121913668
GWAS Ctlg	rs121913668

Merged from

Rs28933101

Max Magnitude

5.7

OMIM	164860
Desc
Variant	0001
Related	also

ClinVar
Risk	rs121913668(C;C)
Alt	rs121913668(C;C)
Reference	Rs121913668(T;T)
Significance	Pathogenic
Disease	Renal cell carcinoma
Variation	info
Gene	MET
CLNDBN	Renal cell carcinoma, papillary, 1
Reversed	0
HGVS	NC_000007.13:g.116418881T>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000014895.21,