rs267607991

Orientation

plus

Stabilized

plus

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

Make rs267607991(G;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47476365

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs267607991
dbSNP (classic)	rs267607991
ClinGen	rs267607991
ebi	rs267607991
HLI	rs267607991
Exac	rs267607991
Gnomad	rs267607991
Varsome	rs267607991
LitVar	rs267607991
Map	rs267607991
PheGenI	rs267607991
Biobank	rs267607991
1000 genomes	rs267607991
hgdp	rs267607991
ensembl	rs267607991
geneview	rs267607991
scholar	rs267607991
google	rs267607991
pharmgkb	rs267607991
gwascentral	rs267607991
openSNP	rs267607991
23andMe	rs267607991
SNPshot	rs267607991
SNPdbe	rs267607991
MSV3d	rs267607991
GWAS Ctlg	rs267607991

Max Magnitude

6

ClinVar
Risk	rs267607991(G;G)
Alt	rs267607991(G;G)
Reference	Rs267607991(A;A)
Significance	Probable-Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47703504A>G
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076349.2,