rs267607956

Orientation

plus

Stabilized

plus

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

Make rs267607956(T;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47463030

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs267607956
dbSNP (classic)	rs267607956
ClinGen	rs267607956
ebi	rs267607956
HLI	rs267607956
Exac	rs267607956
Gnomad	rs267607956
Varsome	rs267607956
LitVar	rs267607956
Map	rs267607956
PheGenI	rs267607956
Biobank	rs267607956
1000 genomes	rs267607956
hgdp	rs267607956
ensembl	rs267607956
geneview	rs267607956
scholar	rs267607956
google	rs267607956
pharmgkb	rs267607956
gwascentral	rs267607956
openSNP	rs267607956
23andMe	rs267607956
SNPshot	rs267607956
SNPdbe	rs267607956
MSV3d	rs267607956
GWAS Ctlg	rs267607956

Max Magnitude

6

ClinVar
Risk	rs267607956(T;T)
Alt	rs267607956(T;T)
Reference	Rs267607956(G;G)
Significance	Probable-Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47690169G>T
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076141.2,