rs121913243

Orientation

plus

Stabilized

plus

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

Make rs121913243(G;G)

Reference

GRCh38 38.1/141

Chromosome

7

Position

116777410

Gene

MET

is a	snp
is	mentioned by
dbSNP	rs121913243
dbSNP (classic)	rs121913243
ClinGen	rs121913243
ebi	rs121913243
HLI	rs121913243
Exac	rs121913243
Gnomad	rs121913243
Varsome	rs121913243
LitVar	rs121913243
Map	rs121913243
PheGenI	rs121913243
Biobank	rs121913243
1000 genomes	rs121913243
hgdp	rs121913243
ensembl	rs121913243
geneview	rs121913243
scholar	rs121913243
google	rs121913243
pharmgkb	rs121913243
gwascentral	rs121913243
openSNP	rs121913243
23andMe	rs121913243
SNPshot	rs121913243
SNPdbe	rs121913243
MSV3d	rs121913243
GWAS Ctlg	rs121913243

Max Magnitude

5.7

OMIM	164860
Desc
Variant	0007
Related	also

ClinVar
Risk	rs121913243(C;C) rs121913243(G;G)
Alt	rs121913243(C;C) rs121913243(G;G)
Reference	Rs121913243(A;A)
Significance	Pathogenic
Disease	Renal cell carcinoma not provided Kidney Carcinoma
Variation	info
Gene	MET
CLNDBN	Renal cell carcinoma, papillary, 1 not provided Kidney Carcinoma
Reversed	0
HGVS	NC_000007.13:g.116417464A>G
CLNSRC	HGMD OMIM Allelic Variant
CLNACC	RCV000014901.26, RCV000079490.4, RCV000433739.1,