rs786202724

Orientation

plus

Stabilized

plus

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

Make rs786202724(A;A)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

116777403

Gene

MET

is a	snp
is	mentioned by
dbSNP	rs786202724
dbSNP (classic)	rs786202724
ClinGen	rs786202724
ebi	rs786202724
HLI	rs786202724
Exac	rs786202724
Gnomad	rs786202724
Varsome	rs786202724
LitVar	rs786202724
Map	rs786202724
PheGenI	rs786202724
Biobank	rs786202724
1000 genomes	rs786202724
hgdp	rs786202724
ensembl	rs786202724
geneview	rs786202724
scholar	rs786202724
google	rs786202724
pharmgkb	rs786202724
gwascentral	rs786202724
openSNP	rs786202724
23andMe	rs786202724
SNPshot	rs786202724
SNPdbe	rs786202724
MSV3d	rs786202724
GWAS Ctlg	rs786202724

Max Magnitude

5.7

ClinVar
Risk	rs786202724(A;A)
Alt	rs786202724(A;A)
Reference	Rs786202724(G;G)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome Neoplasm Carcinoma
Variation	info
Gene	MET
CLNDBN	Hereditary cancer-predisposing syndrome Neoplasm Carcinoma
Reversed	0
HGVS	NC_000007.13:g.116417457G>A
CLNSRC
CLNACC	RCV000165679.1, RCV000425188.1, RCV000443267.1,