rs63750857

Orientation

plus

Stabilized

plus

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

Make rs63750857(T;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47480773

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63750857
dbSNP (classic)	rs63750857
ClinGen	rs63750857
ebi	rs63750857
HLI	rs63750857
Exac	rs63750857
Gnomad	rs63750857
Varsome	rs63750857
LitVar	rs63750857
Map	rs63750857
PheGenI	rs63750857
Biobank	rs63750857
1000 genomes	rs63750857
hgdp	rs63750857
ensembl	rs63750857
geneview	rs63750857
scholar	rs63750857
google	rs63750857
pharmgkb	rs63750857
gwascentral	rs63750857
openSNP	rs63750857
23andMe	rs63750857
SNPshot	rs63750857
SNPdbe	rs63750857
MSV3d	rs63750857
GWAS Ctlg	rs63750857

Max Magnitude

6

ClinVar
Risk	rs63750857(T;T)
Alt	rs63750857(T;T)
Reference	Rs63750857(C;C)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47707912C>T
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076498.2,