rs63749983

Orientation

plus

Stabilized

plus

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

Make rs63749983(-;-)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47478449

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63749983
dbSNP (classic)	rs63749983
ClinGen	rs63749983
ebi	rs63749983
HLI	rs63749983
Exac	rs63749983
Gnomad	rs63749983
Varsome	rs63749983
LitVar	rs63749983
Map	rs63749983
PheGenI	rs63749983
Biobank	rs63749983
1000 genomes	rs63749983
hgdp	rs63749983
ensembl	rs63749983
geneview	rs63749983
scholar	rs63749983
google	rs63749983
pharmgkb	rs63749983
gwascentral	rs63749983
openSNP	rs63749983
23andMe	rs63749983
SNPshot	rs63749983
SNPdbe	rs63749983
MSV3d	rs63749983
GWAS Ctlg	rs63749983

Max Magnitude

6

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

ClinVar
Risk	rs63749983(-;-)
Alt	rs63749983(-;-)
Reference	Rs63749983(T;T)
Significance	Pathogenic
Disease	Lynch syndrome Hereditary cancer-predisposing syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000002.11:g.47705588delT
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076465.2, RCV000219933.2,