rs267607920

Orientation

plus

Stabilized

plus

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

Make rs267607920(-;-)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47408452

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs267607920
dbSNP (classic)	rs267607920
ClinGen	rs267607920
ebi	rs267607920
HLI	rs267607920
Exac	rs267607920
Gnomad	rs267607920
Varsome	rs267607920
LitVar	rs267607920
Map	rs267607920
PheGenI	rs267607920
Biobank	rs267607920
1000 genomes	rs267607920
hgdp	rs267607920
ensembl	rs267607920
geneview	rs267607920
scholar	rs267607920
google	rs267607920
pharmgkb	rs267607920
gwascentral	rs267607920
openSNP	rs267607920
23andMe	rs267607920
SNPshot	rs267607920
SNPdbe	rs267607920
MSV3d	rs267607920
GWAS Ctlg	rs267607920

Max Magnitude

6

aka both c.264dupT as well as c.263_264delTT

ClinVar
Risk	rs267607920(-;-)
Alt	rs267607920(-;-)
Reference	Rs267607920(TT;TT)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47635591_47635592delTT
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076531.2,