rs121913670

Orientation

plus

Stabilized

plus

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

Make rs121913670(A;A)

Reference

GRCh38 38.1/141

Chromosome

7

Position

116783329

Gene

MET

is a	snp
is	mentioned by
dbSNP	rs121913670
dbSNP (classic)	rs121913670
ClinGen	rs121913670
ebi	rs121913670
HLI	rs121913670
Exac	rs121913670
Gnomad	rs121913670
Varsome	rs121913670
LitVar	rs121913670
Map	rs121913670
PheGenI	rs121913670
Biobank	rs121913670
1000 genomes	rs121913670
hgdp	rs121913670
ensembl	rs121913670
geneview	rs121913670
scholar	rs121913670
google	rs121913670
pharmgkb	rs121913670
gwascentral	rs121913670
openSNP	rs121913670
23andMe	rs121913670
SNPshot	rs121913670
SNPdbe	rs121913670
MSV3d	rs121913670
GWAS Ctlg	rs121913670

Merged from

Rs28932776

Max Magnitude

5.7

OMIM	164860
Desc
Variant	0003
Related	also

ClinVar
Risk	rs121913670(A;A)
Alt	rs121913670(A;A)
Reference	Rs121913670(G;G)
Significance	Pathogenic
Disease	Renal cell carcinoma Hereditary cancer-predisposing syndrome
Variation	info
Gene	MET
CLNDBN	Renal cell carcinoma, papillary, 1 Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000007.13:g.116423383G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000014897.25, RCV000221989.1,