rs121913677

Orientation

plus

Stabilized

plus

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

Make rs121913677(A;G)

Make rs121913677(G;G)

Reference

GRCh38 38.1/141

Chromosome

7

Position

116783402

Gene

MET

is a	snp
is	mentioned by
dbSNP	rs121913677
dbSNP (classic)	rs121913677
ClinGen	rs121913677
ebi	rs121913677
HLI	rs121913677
Exac	rs121913677
Gnomad	rs121913677
Varsome	rs121913677
LitVar	rs121913677
Map	rs121913677
PheGenI	rs121913677
Biobank	rs121913677
1000 genomes	rs121913677
hgdp	rs121913677
ensembl	rs121913677
geneview	rs121913677
scholar	rs121913677
google	rs121913677
pharmgkb	rs121913677
gwascentral	rs121913677
openSNP	rs121913677
23andMe	rs121913677
SNPshot	rs121913677
SNPdbe	rs121913677
MSV3d	rs121913677
GWAS Ctlg	rs121913677

Max Magnitude

0

OMIM	164860
Desc
Variant	0010
Related	also

ClinVar
Risk	rs121913677(G;G)
Alt	rs121913677(G;G)
Reference	Rs121913677(A;A)
Significance	Pathogenic
Disease	Childhood hepatocellular carcinoma
Variation	info
Gene	MET
CLNDBN	Childhood hepatocellular carcinoma
Reversed	0
HGVS	NC_000007.13:g.116423456A>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000014904.6,