rs786204321

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar
(C;T)	6	Lynch syndrome

Make rs786204321(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

47475249

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs786204321
dbSNP (classic)	rs786204321
ClinGen	rs786204321
ebi	rs786204321
HLI	rs786204321
Exac	rs786204321
Gnomad	rs786204321
Varsome	rs786204321
LitVar	rs786204321
Map	rs786204321
PheGenI	rs786204321
Biobank	rs786204321
1000 genomes	rs786204321
hgdp	rs786204321
ensembl	rs786204321
geneview	rs786204321
scholar	rs786204321
google	rs786204321
pharmgkb	rs786204321
gwascentral	rs786204321
openSNP	rs786204321
23andMe	rs786204321
SNPshot	rs786204321
SNPdbe	rs786204321
MSV3d	rs786204321
GWAS Ctlg	rs786204321

Max Magnitude

6

ClinVar
Risk	rs786204321(T;T)
Alt	rs786204321(T;T)
Reference	Rs786204321(C;C)
Significance	Pathogenic
Disease	Lynch syndrome not provided
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome not provided
Reversed	0
HGVS	NC_000002.11:g.47702388C>T
CLNSRC	Children's Hospital of Eastern Ontario
CLNACC	RCV000168729.2, RCV000480108.1,