rs1057520030

Orientation

plus

Stabilized

plus

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

Make rs1057520030(A;T)

Make rs1057520030(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

116777427

Gene

MET

is a	snp
is	mentioned by
dbSNP	rs1057520030
dbSNP (classic)	rs1057520030
ClinGen	rs1057520030
ebi	rs1057520030
HLI	rs1057520030
Exac	rs1057520030
Gnomad	rs1057520030
Varsome	rs1057520030
LitVar	rs1057520030
Map	rs1057520030
PheGenI	rs1057520030
Biobank	rs1057520030
1000 genomes	rs1057520030
hgdp	rs1057520030
ensembl	rs1057520030
geneview	rs1057520030
scholar	rs1057520030
google	rs1057520030
pharmgkb	rs1057520030
gwascentral	rs1057520030
openSNP	rs1057520030
23andMe	rs1057520030
SNPshot	rs1057520030
SNPdbe	rs1057520030
MSV3d	rs1057520030
GWAS Ctlg	rs1057520030

Max Magnitude

0

ClinVar
Risk	rs1057520030(T;T)
Alt	rs1057520030(T;T)
Reference	Rs1057520030(A;A)
Significance	Probable-Pathogenic
Disease	Carcinoma
Variation	info
Gene	MET
CLNDBN	Carcinoma
Reversed	0
HGVS	NC_000007.13:g.116417481A>T
CLNSRC
CLNACC	RCV000418101.1,