rs267607911

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;A)	0	common in clinvar

Make rs267607911(A;T)

Make rs267607911(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

2

Position

47403192

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs267607911
dbSNP (classic)	rs267607911
ClinGen	rs267607911
ebi	rs267607911
HLI	rs267607911
Exac	rs267607911
Gnomad	rs267607911
Varsome	rs267607911
LitVar	rs267607911
Map	rs267607911
PheGenI	rs267607911
Biobank	rs267607911
1000 genomes	rs267607911
hgdp	rs267607911
ensembl	rs267607911
geneview	rs267607911
scholar	rs267607911
google	rs267607911
pharmgkb	rs267607911
gwascentral	rs267607911
openSNP	rs267607911
23andMe	rs267607911
SNPshot	rs267607911
SNPdbe	rs267607911
MSV3d	rs267607911
GWAS Ctlg	rs267607911

Max Magnitude

0

ClinVar
Risk	rs267607911(C;C) rs267607911(G;G) rs267607911(T;T)
Alt	rs267607911(C;C) rs267607911(G;G) rs267607911(T;T)
Reference	Rs267607911(A;A)
Significance	Probable-Pathogenic
Disease	Lynch syndrome Hereditary cancer-predisposing syndrome Lynch syndrome I not specified
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome Hereditary cancer-predisposing syndrome Lynch syndrome I not specified
Reversed	0
HGVS	NC_000002.11:g.47630331A>C; NC_000002.11:g.47630331A>G; NC_000002.11:g.47630331A>T
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076334.4, RCV000160588.6, RCV000409939.1, RCV000076335.2, RCV000165763.1, RCV000172811.1, RCV000235433.1, RCV000076336.3,