rs63750843

Orientation

plus

Stabilized

plus

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

Make rs63750843(C;G)

Make rs63750843(G;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47410235

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63750843
dbSNP (classic)	rs63750843
ClinGen	rs63750843
ebi	rs63750843
HLI	rs63750843
Exac	rs63750843
Gnomad	rs63750843
Varsome	rs63750843
LitVar	rs63750843
Map	rs63750843
PheGenI	rs63750843
Biobank	rs63750843
1000 genomes	rs63750843
hgdp	rs63750843
ensembl	rs63750843
geneview	rs63750843
scholar	rs63750843
google	rs63750843
pharmgkb	rs63750843
gwascentral	rs63750843
openSNP	rs63750843
23andMe	rs63750843
SNPshot	rs63750843
SNPdbe	rs63750843
MSV3d	rs63750843
GWAS Ctlg	rs63750843

Max Magnitude

6

ClinVar
Risk	rs63750843(G;G) rs63750843(T;T)
Alt	rs63750843(G;G) rs63750843(T;T)
Reference	Rs63750843(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.47637374C>G; NC_000002.11:g.47637374C>T
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000204442.1, RCV000214137.1, RCV000076621.2, RCV000236121.2, RCV000491287.1,