rs786203704

Orientation

plus

Stabilized

plus

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

Make rs786203704(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

47475068

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs786203704
dbSNP (classic)	rs786203704
ClinGen	rs786203704
ebi	rs786203704
HLI	rs786203704
Exac	rs786203704
Gnomad	rs786203704
Varsome	rs786203704
LitVar	rs786203704
Map	rs786203704
PheGenI	rs786203704
Biobank	rs786203704
1000 genomes	rs786203704
hgdp	rs786203704
ensembl	rs786203704
geneview	rs786203704
scholar	rs786203704
google	rs786203704
pharmgkb	rs786203704
gwascentral	rs786203704
openSNP	rs786203704
23andMe	rs786203704
SNPshot	rs786203704
SNPdbe	rs786203704
MSV3d	rs786203704
GWAS Ctlg	rs786203704

Max Magnitude

6

ClinVar
Risk	rs786203704(G;G)
Alt	rs786203704(G;G)
Reference	Rs786203704(-;-)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	MSH2
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000002.11:g.47702207dupG
CLNSRC
CLNACC	RCV000167124.1,