rs63750037

Orientation

plus

Stabilized

plus

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

Make rs63750037(T;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47410274

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63750037
dbSNP (classic)	rs63750037
ClinGen	rs63750037
ebi	rs63750037
HLI	rs63750037
Exac	rs63750037
Gnomad	rs63750037
Varsome	rs63750037
LitVar	rs63750037
Map	rs63750037
PheGenI	rs63750037
Biobank	rs63750037
1000 genomes	rs63750037
hgdp	rs63750037
ensembl	rs63750037
geneview	rs63750037
scholar	rs63750037
google	rs63750037
pharmgkb	rs63750037
gwascentral	rs63750037
openSNP	rs63750037
23andMe	rs63750037
SNPshot	rs63750037
SNPdbe	rs63750037
MSV3d	rs63750037
GWAS Ctlg	rs63750037

Max Magnitude

6

ClinVar
Risk	rs63750037(T;T)
Alt	rs63750037(T;T)
Reference	Rs63750037(C;C)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47637413C>T
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076634.2,