rs63750496

Orientation

plus

Stabilized

plus

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

Make rs63750496(C;C)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47429809

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63750496
dbSNP (classic)	rs63750496
ClinGen	rs63750496
ebi	rs63750496
HLI	rs63750496
Exac	rs63750496
Gnomad	rs63750496
Varsome	rs63750496
LitVar	rs63750496
Map	rs63750496
PheGenI	rs63750496
Biobank	rs63750496
1000 genomes	rs63750496
hgdp	rs63750496
ensembl	rs63750496
geneview	rs63750496
scholar	rs63750496
google	rs63750496
pharmgkb	rs63750496
gwascentral	rs63750496
openSNP	rs63750496
23andMe	rs63750496
SNPshot	rs63750496
SNPdbe	rs63750496
MSV3d	rs63750496
GWAS Ctlg	rs63750496

Max Magnitude

6

ClinVar
Risk	rs63750496(C;C)
Alt	rs63750496(C;C)
Reference	Rs63750496(-;-)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47656948dupC
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076047.2,