rs63750636

Orientation

plus

Stabilized

plus

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

Make rs63750636(T;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47476492

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63750636
dbSNP (classic)	rs63750636
ClinGen	rs63750636
ebi	rs63750636
HLI	rs63750636
Exac	rs63750636
Gnomad	rs63750636
Varsome	rs63750636
LitVar	rs63750636
Map	rs63750636
PheGenI	rs63750636
Biobank	rs63750636
1000 genomes	rs63750636
hgdp	rs63750636
ensembl	rs63750636
geneview	rs63750636
scholar	rs63750636
google	rs63750636
pharmgkb	rs63750636
gwascentral	rs63750636
openSNP	rs63750636
23andMe	rs63750636
SNPshot	rs63750636
SNPdbe	rs63750636
MSV3d	rs63750636
GWAS Ctlg	rs63750636

Max Magnitude

6

Prevalence and Spectrum of Germline Cancer Susceptibility Gene Mutations Among Patients With Early-Onset Colorectal Cancer [PMID 27978560]

ClinVar
Risk	rs63750636(T;T)
Alt	rs63750636(T;T)
Reference	Rs63750636(C;C)
Significance	Pathogenic
Disease	Lynch syndrome Hereditary cancer-predisposing syndrome not provided
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome Hereditary cancer-predisposing syndrome not provided
Reversed	0
HGVS	NC_000002.11:g.47703631C>T
CLNSRC	Children's Hospital of Eastern Ontario International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076405.3, RCV000129341.4, RCV000202062.3,