rs63750682

Orientation

plus

Stabilized

plus

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

Make rs63750682(-;-)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47410314

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63750682
dbSNP (classic)	rs63750682
ClinGen	rs63750682
ebi	rs63750682
HLI	rs63750682
Exac	rs63750682
Gnomad	rs63750682
Varsome	rs63750682
LitVar	rs63750682
Map	rs63750682
PheGenI	rs63750682
Biobank	rs63750682
1000 genomes	rs63750682
hgdp	rs63750682
ensembl	rs63750682
geneview	rs63750682
scholar	rs63750682
google	rs63750682
pharmgkb	rs63750682
gwascentral	rs63750682
openSNP	rs63750682
23andMe	rs63750682
SNPshot	rs63750682
SNPdbe	rs63750682
MSV3d	rs63750682
GWAS Ctlg	rs63750682

Max Magnitude

6

ClinVar
Risk	rs63750682(-;-)
Alt	rs63750682(-;-)
Reference	Rs63750682(C;C)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47637453delC
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076646.2,