rs63750675

Orientation

plus

Stabilized

plus

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

Make rs63750675(-;-)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47466774

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63750675
dbSNP (classic)	rs63750675
ClinGen	rs63750675
ebi	rs63750675
HLI	rs63750675
Exac	rs63750675
Gnomad	rs63750675
Varsome	rs63750675
LitVar	rs63750675
Map	rs63750675
PheGenI	rs63750675
Biobank	rs63750675
1000 genomes	rs63750675
hgdp	rs63750675
ensembl	rs63750675
geneview	rs63750675
scholar	rs63750675
google	rs63750675
pharmgkb	rs63750675
gwascentral	rs63750675
openSNP	rs63750675
23andMe	rs63750675
SNPshot	rs63750675
SNPdbe	rs63750675
MSV3d	rs63750675
GWAS Ctlg	rs63750675

Max Magnitude

6

ClinVar
Risk	rs63750675(-;-)
Alt	rs63750675(-;-)
Reference	Rs63750675(G;G)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47693913delG
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076207.2,