rs63750103

Orientation

plus

Stabilized

plus

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

Make rs63750103(-;-)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47475025

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63750103
dbSNP (classic)	rs63750103
ClinGen	rs63750103
ebi	rs63750103
HLI	rs63750103
Exac	rs63750103
Gnomad	rs63750103
Varsome	rs63750103
LitVar	rs63750103
Map	rs63750103
PheGenI	rs63750103
Biobank	rs63750103
1000 genomes	rs63750103
hgdp	rs63750103
ensembl	rs63750103
geneview	rs63750103
scholar	rs63750103
google	rs63750103
pharmgkb	rs63750103
gwascentral	rs63750103
openSNP	rs63750103
23andMe	rs63750103
SNPshot	rs63750103
SNPdbe	rs63750103
MSV3d	rs63750103
GWAS Ctlg	rs63750103

Max Magnitude

6

ClinVar
Risk	rs63750103(-;-)
Alt	rs63750103(-;-)
Reference	Rs63750103(G;G)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47702164delG
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076278.2,