rs63750551

Orientation

plus

Stabilized

plus

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

Make rs63750551(-;-)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47410257

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63750551
dbSNP (classic)	rs63750551
ClinGen	rs63750551
ebi	rs63750551
HLI	rs63750551
Exac	rs63750551
Gnomad	rs63750551
Varsome	rs63750551
LitVar	rs63750551
Map	rs63750551
PheGenI	rs63750551
Biobank	rs63750551
1000 genomes	rs63750551
hgdp	rs63750551
ensembl	rs63750551
geneview	rs63750551
scholar	rs63750551
google	rs63750551
pharmgkb	rs63750551
gwascentral	rs63750551
openSNP	rs63750551
23andMe	rs63750551
SNPshot	rs63750551
SNPdbe	rs63750551
MSV3d	rs63750551
GWAS Ctlg	rs63750551

Max Magnitude

6

ClinVar
Risk	rs63750551(-;-)
Alt	rs63750551(-;-)
Reference	Rs63750551(AA;AA)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47637396_47637397delAA
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076633.2,