rs267607689

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, pathogenic mutation

Make rs267607689(A;A)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47410373

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs267607689
dbSNP (classic)	rs267607689
ClinGen	rs267607689
ebi	rs267607689
HLI	rs267607689
Exac	rs267607689
Gnomad	rs267607689
Varsome	rs267607689
LitVar	rs267607689
Map	rs267607689
PheGenI	rs267607689
Biobank	rs267607689
1000 genomes	rs267607689
hgdp	rs267607689
ensembl	rs267607689
geneview	rs267607689
scholar	rs267607689
google	rs267607689
pharmgkb	rs267607689
gwascentral	rs267607689
openSNP	rs267607689
23andMe	rs267607689
SNPshot	rs267607689
SNPdbe	rs267607689
MSV3d	rs267607689
GWAS Ctlg	rs267607689

Max Magnitude

6

ClinVar
Risk	rs267607689(A;A) rs267607689(T;T)
Alt	rs267607689(A;A) rs267607689(T;T)
Reference	Rs267607689(G;G)
Significance	Pathogenic
Disease	Lynch syndrome Hereditary cancer-predisposing syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000002.11:g.47637512G>A; NC_000002.11:g.47637512G>T
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076659.2, RCV000491616.1, RCV000076660.2, RCV000220374.1,