rs786204050

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;G)	6	Lynch syndrome
(G;G)	0	common in clinvar

Make rs786204050(-;-)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

47478342

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs786204050
dbSNP (classic)	rs786204050
ClinGen	rs786204050
ebi	rs786204050
HLI	rs786204050
Exac	rs786204050
Gnomad	rs786204050
Varsome	rs786204050
LitVar	rs786204050
Map	rs786204050
PheGenI	rs786204050
Biobank	rs786204050
1000 genomes	rs786204050
hgdp	rs786204050
ensembl	rs786204050
geneview	rs786204050
scholar	rs786204050
google	rs786204050
pharmgkb	rs786204050
gwascentral	rs786204050
openSNP	rs786204050
23andMe	rs786204050
SNPshot	rs786204050
SNPdbe	rs786204050
MSV3d	rs786204050
GWAS Ctlg	rs786204050

Max Magnitude

6

ClinVar
Risk	rs786204050(-;-)
Alt	rs786204050(-;-)
Reference	Rs786204050(G;G)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47705481delG
CLNSRC
CLNACC	RCV000167895.1,