rs267607917

Orientation

plus

Stabilized

plus

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

Make rs267607917(G;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47408399

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs267607917
dbSNP (classic)	rs267607917
ClinGen	rs267607917
ebi	rs267607917
HLI	rs267607917
Exac	rs267607917
Gnomad	rs267607917
Varsome	rs267607917
LitVar	rs267607917
Map	rs267607917
PheGenI	rs267607917
Biobank	rs267607917
1000 genomes	rs267607917
hgdp	rs267607917
ensembl	rs267607917
geneview	rs267607917
scholar	rs267607917
google	rs267607917
pharmgkb	rs267607917
gwascentral	rs267607917
openSNP	rs267607917
23andMe	rs267607917
SNPshot	rs267607917
SNPdbe	rs267607917
MSV3d	rs267607917
GWAS Ctlg	rs267607917

Max Magnitude

6

ClinVar
Risk	rs267607917(G;G)
Alt	rs267607917(G;G)
Reference	Rs267607917(A;A)
Significance	Probable-Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47635538A>G
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076395.2,