rs267607977

Orientation

plus

Stabilized

plus

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

Make rs267607977(A;A)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47475036

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs267607977
dbSNP (classic)	rs267607977
ClinGen	rs267607977
ebi	rs267607977
HLI	rs267607977
Exac	rs267607977
Gnomad	rs267607977
Varsome	rs267607977
LitVar	rs267607977
Map	rs267607977
PheGenI	rs267607977
Biobank	rs267607977
1000 genomes	rs267607977
hgdp	rs267607977
ensembl	rs267607977
geneview	rs267607977
scholar	rs267607977
google	rs267607977
pharmgkb	rs267607977
gwascentral	rs267607977
openSNP	rs267607977
23andMe	rs267607977
SNPshot	rs267607977
SNPdbe	rs267607977
MSV3d	rs267607977
GWAS Ctlg	rs267607977

Max Magnitude

6

ClinVar
Risk	rs267607977(A;A)
Alt	rs267607977(A;A)
Reference	Rs267607977(-;-)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47702175_47702176insA
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076280.2,