rs786203604

Orientation

plus

Stabilized

plus

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

Make rs786203604(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

47414389

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs786203604
dbSNP (classic)	rs786203604
ClinGen	rs786203604
ebi	rs786203604
HLI	rs786203604
Exac	rs786203604
Gnomad	rs786203604
Varsome	rs786203604
LitVar	rs786203604
Map	rs786203604
PheGenI	rs786203604
Biobank	rs786203604
1000 genomes	rs786203604
hgdp	rs786203604
ensembl	rs786203604
geneview	rs786203604
scholar	rs786203604
google	rs786203604
pharmgkb	rs786203604
gwascentral	rs786203604
openSNP	rs786203604
23andMe	rs786203604
SNPshot	rs786203604
SNPdbe	rs786203604
MSV3d	rs786203604
GWAS Ctlg	rs786203604

Max Magnitude

6

ClinVar
Risk	rs786203604(G;G)
Alt	rs786203604(G;G)
Reference	Rs786203604(-;-)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	MSH2
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000002.11:g.47641528dupG
CLNSRC
CLNACC	RCV000166990.1,