rs63750644

Orientation

plus

Stabilized

plus

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

Make rs63750644(-;-)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47403336

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63750644
dbSNP (classic)	rs63750644
ClinGen	rs63750644
ebi	rs63750644
HLI	rs63750644
Exac	rs63750644
Gnomad	rs63750644
Varsome	rs63750644
LitVar	rs63750644
Map	rs63750644
PheGenI	rs63750644
Biobank	rs63750644
1000 genomes	rs63750644
hgdp	rs63750644
ensembl	rs63750644
geneview	rs63750644
scholar	rs63750644
google	rs63750644
pharmgkb	rs63750644
gwascentral	rs63750644
openSNP	rs63750644
23andMe	rs63750644
SNPshot	rs63750644
SNPdbe	rs63750644
MSV3d	rs63750644
GWAS Ctlg	rs63750644

Max Magnitude

6

ClinVar
Risk	rs63750644(-;-)
Alt	rs63750644(-;-)
Reference	Rs63750644(G;G)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47630475delG
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076169.2,