rs267608010

Orientation

plus

Stabilized

plus

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

Make rs267608010(A;A)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47478520

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs267608010
dbSNP (classic)	rs267608010
ClinGen	rs267608010
ebi	rs267608010
HLI	rs267608010
Exac	rs267608010
Gnomad	rs267608010
Varsome	rs267608010
LitVar	rs267608010
Map	rs267608010
PheGenI	rs267608010
Biobank	rs267608010
1000 genomes	rs267608010
hgdp	rs267608010
ensembl	rs267608010
geneview	rs267608010
scholar	rs267608010
google	rs267608010
pharmgkb	rs267608010
gwascentral	rs267608010
openSNP	rs267608010
23andMe	rs267608010
SNPshot	rs267608010
SNPdbe	rs267608010
MSV3d	rs267608010
GWAS Ctlg	rs267608010

Max Magnitude

6

ClinVar
Risk	rs267608010(A;A)
Alt	rs267608010(A;A)
Reference	Rs267608010(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.47705659G>A
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076478.2, RCV000479442.1, RCV000491889.1,