rs63750458

Orientation

plus

Stabilized

plus

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

Make rs63750458(G;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47408552

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63750458
dbSNP (classic)	rs63750458
ClinGen	rs63750458
ebi	rs63750458
HLI	rs63750458
Exac	rs63750458
Gnomad	rs63750458
Varsome	rs63750458
LitVar	rs63750458
Map	rs63750458
PheGenI	rs63750458
Biobank	rs63750458
1000 genomes	rs63750458
hgdp	rs63750458
ensembl	rs63750458
geneview	rs63750458
scholar	rs63750458
google	rs63750458
pharmgkb	rs63750458
gwascentral	rs63750458
openSNP	rs63750458
23andMe	rs63750458
SNPshot	rs63750458
SNPdbe	rs63750458
MSV3d	rs63750458
GWAS Ctlg	rs63750458

Max Magnitude

6

ClinVar
Risk	rs63750458(G;G)
Alt	rs63750458(G;G)
Reference	Rs63750458(T;T)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47635691T>G
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076572.2,