rs267607961

Orientation

plus

Stabilized

plus

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

Make rs267607961(-;-)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47463089

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs267607961
dbSNP (classic)	rs267607961
ClinGen	rs267607961
ebi	rs267607961
HLI	rs267607961
Exac	rs267607961
Gnomad	rs267607961
Varsome	rs267607961
LitVar	rs267607961
Map	rs267607961
PheGenI	rs267607961
Biobank	rs267607961
1000 genomes	rs267607961
hgdp	rs267607961
ensembl	rs267607961
geneview	rs267607961
scholar	rs267607961
google	rs267607961
pharmgkb	rs267607961
gwascentral	rs267607961
openSNP	rs267607961
23andMe	rs267607961
SNPshot	rs267607961
SNPdbe	rs267607961
MSV3d	rs267607961
GWAS Ctlg	rs267607961

Max Magnitude

6

ClinVar
Risk	rs267607961(-;-)
Alt	rs267607961(-;-)
Reference	Rs267607961(AAGAG;AAGAG)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47690228_47690232delGAGAA
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076163.2,