rs267607691

Orientation

plus

Stabilized

plus

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

Make rs267607691(CT;CT)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47475046

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs267607691
dbSNP (classic)	rs267607691
ClinGen	rs267607691
ebi	rs267607691
HLI	rs267607691
Exac	rs267607691
Gnomad	rs267607691
Varsome	rs267607691
LitVar	rs267607691
Map	rs267607691
PheGenI	rs267607691
Biobank	rs267607691
1000 genomes	rs267607691
hgdp	rs267607691
ensembl	rs267607691
geneview	rs267607691
scholar	rs267607691
google	rs267607691
pharmgkb	rs267607691
gwascentral	rs267607691
openSNP	rs267607691
23andMe	rs267607691
SNPshot	rs267607691
SNPdbe	rs267607691
MSV3d	rs267607691
GWAS Ctlg	rs267607691

Max Magnitude

6

ClinVar
Risk	rs267607691(CT;CT)
Alt	rs267607691(CT;CT)
Reference	Rs267607691(-;-)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47702185_47702186insCT
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076284.2,