rs121913675

Orientation

plus

Stabilized

plus

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

Make rs121913675(C;T)

Make rs121913675(T;T)

Reference

GRCh38 38.1/141

Chromosome

7

Position

116778953

Gene

MET

is a	snp
is	mentioned by
dbSNP	rs121913675
dbSNP (classic)	rs121913675
ClinGen	rs121913675
ebi	rs121913675
HLI	rs121913675
Exac	rs121913675
Gnomad	rs121913675
Varsome	rs121913675
LitVar	rs121913675
Map	rs121913675
PheGenI	rs121913675
Biobank	rs121913675
1000 genomes	rs121913675
hgdp	rs121913675
ensembl	rs121913675
geneview	rs121913675
scholar	rs121913675
google	rs121913675
pharmgkb	rs121913675
gwascentral	rs121913675
openSNP	rs121913675
23andMe	rs121913675
SNPshot	rs121913675
SNPdbe	rs121913675
MSV3d	rs121913675
GWAS Ctlg	rs121913675

Max Magnitude

0

OMIM	164860
Desc
Variant	0008
Related	also

ClinVar
Risk	rs121913675(T;T)
Alt	rs121913675(T;T)
Reference	Rs121913675(C;C)
Significance	Pathogenic
Disease	Childhood hepatocellular carcinoma
Variation	info
Gene	MET
CLNDBN	Childhood hepatocellular carcinoma
Reversed	0
HGVS	NC_000007.13:g.116419007C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000014902.6,