rs267607914

Orientation

plus

Stabilized

plus

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

Make rs267607914(A;A)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47408400

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs267607914
dbSNP (classic)	rs267607914
ClinGen	rs267607914
ebi	rs267607914
HLI	rs267607914
Exac	rs267607914
Gnomad	rs267607914
Varsome	rs267607914
LitVar	rs267607914
Map	rs267607914
PheGenI	rs267607914
Biobank	rs267607914
1000 genomes	rs267607914
hgdp	rs267607914
ensembl	rs267607914
geneview	rs267607914
scholar	rs267607914
google	rs267607914
pharmgkb	rs267607914
gwascentral	rs267607914
openSNP	rs267607914
23andMe	rs267607914
SNPshot	rs267607914
SNPdbe	rs267607914
MSV3d	rs267607914
GWAS Ctlg	rs267607914

Max Magnitude

6

ClinVar
Risk	rs267607914(A;A)
Alt	rs267607914(A;A)
Reference	Rs267607914(G;G)
Significance	Pathogenic
Disease	Lynch syndrome not provided Hereditary cancer-predisposing syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome not provided Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000002.11:g.47635539G>A
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076394.2, RCV000202270.1, RCV000218216.2,