rs63750640

Orientation

plus

Stabilized

plus

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

Make rs63750640(C;C)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47414405

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63750640
dbSNP (classic)	rs63750640
ClinGen	rs63750640
ebi	rs63750640
HLI	rs63750640
Exac	rs63750640
Gnomad	rs63750640
Varsome	rs63750640
LitVar	rs63750640
Map	rs63750640
PheGenI	rs63750640
Biobank	rs63750640
1000 genomes	rs63750640
hgdp	rs63750640
ensembl	rs63750640
geneview	rs63750640
scholar	rs63750640
google	rs63750640
pharmgkb	rs63750640
gwascentral	rs63750640
openSNP	rs63750640
23andMe	rs63750640
SNPshot	rs63750640
SNPdbe	rs63750640
MSV3d	rs63750640
GWAS Ctlg	rs63750640

Max Magnitude

6

ClinVar
Risk	rs63750640(C;C) rs63750640(G;G)
Alt	rs63750640(C;C) rs63750640(G;G)
Reference	Rs63750640(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.47641544T>C; NC_000002.11:g.47641544T>G
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076750.2, RCV000491370.1, RCV000076751.2,