rs63750199

Orientation

plus

Stabilized

plus

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

Make rs63750199(-;-)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47403395

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63750199
dbSNP (classic)	rs63750199
ClinGen	rs63750199
ebi	rs63750199
HLI	rs63750199
Exac	rs63750199
Gnomad	rs63750199
Varsome	rs63750199
LitVar	rs63750199
Map	rs63750199
PheGenI	rs63750199
Biobank	rs63750199
1000 genomes	rs63750199
hgdp	rs63750199
ensembl	rs63750199
geneview	rs63750199
scholar	rs63750199
google	rs63750199
pharmgkb	rs63750199
gwascentral	rs63750199
openSNP	rs63750199
23andMe	rs63750199
SNPshot	rs63750199
SNPdbe	rs63750199
MSV3d	rs63750199
GWAS Ctlg	rs63750199

Max Magnitude

6

ClinVar
Risk	rs63750199(-;-)
Alt	rs63750199(-;-)
Reference	Rs63750199(G;G)
Significance	Pathogenic
Disease	Lynch syndrome Hereditary cancer-predisposing syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000002.11:g.47630534delG
CLNSRC	Children's Hospital of Eastern Ontario International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076373.2, RCV000491774.1,