rs63750267

Orientation

plus

Stabilized

plus

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

Make rs63750267(T;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47429794

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63750267
dbSNP (classic)	rs63750267
ClinGen	rs63750267
ebi	rs63750267
HLI	rs63750267
Exac	rs63750267
Gnomad	rs63750267
Varsome	rs63750267
LitVar	rs63750267
Map	rs63750267
PheGenI	rs63750267
Biobank	rs63750267
1000 genomes	rs63750267
hgdp	rs63750267
ensembl	rs63750267
geneview	rs63750267
scholar	rs63750267
google	rs63750267
pharmgkb	rs63750267
gwascentral	rs63750267
openSNP	rs63750267
23andMe	rs63750267
SNPshot	rs63750267
SNPdbe	rs63750267
MSV3d	rs63750267
GWAS Ctlg	rs63750267

Max Magnitude

6

ClinVar
Risk	rs63750267(G;G) rs63750267(T;T)
Alt	rs63750267(G;G) rs63750267(T;T)
Reference	Rs63750267(C;C)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47656933C>T
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076045.2,