rs121913676

Orientation

plus

Stabilized

plus

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

Make rs121913676(A;A)

Make rs121913676(A;G)

Reference

GRCh38 38.1/141

Chromosome

7

Position

116783421

Gene

MET

is a	snp
is	mentioned by
dbSNP	rs121913676
dbSNP (classic)	rs121913676
ClinGen	rs121913676
ebi	rs121913676
HLI	rs121913676
Exac	rs121913676
Gnomad	rs121913676
Varsome	rs121913676
LitVar	rs121913676
Map	rs121913676
PheGenI	rs121913676
Biobank	rs121913676
1000 genomes	rs121913676
hgdp	rs121913676
ensembl	rs121913676
geneview	rs121913676
scholar	rs121913676
google	rs121913676
pharmgkb	rs121913676
gwascentral	rs121913676
openSNP	rs121913676
23andMe	rs121913676
SNPshot	rs121913676
SNPdbe	rs121913676
MSV3d	rs121913676
GWAS Ctlg	rs121913676

Max Magnitude

0

OMIM	164860
Desc
Variant	0009
Related	also

ClinVar
Risk	rs121913676(A;A) rs121913676(C;C) rs121913676(T;T)
Alt	rs121913676(A;A) rs121913676(C;C) rs121913676(T;T)
Reference	Rs121913676(G;G)
Significance	Pathogenic
Disease	Childhood hepatocellular carcinoma Neoplasm
Variation	info
Gene	MET
CLNDBN	Childhood hepatocellular carcinoma Neoplasm
Reversed	0
HGVS	NC_000007.13:g.116423475G>A; NC_000007.13:g.116423475G>C; NC_000007.13:g.116423475G>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000014903.6, RCV000427546.1, RCV000438241.1, RCV000419338.1,