rs267607955

Orientation

plus

Stabilized

plus

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

Make rs267607955(-;-)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47445616

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs267607955
dbSNP (classic)	rs267607955
ClinGen	rs267607955
ebi	rs267607955
HLI	rs267607955
Exac	rs267607955
Gnomad	rs267607955
Varsome	rs267607955
LitVar	rs267607955
Map	rs267607955
PheGenI	rs267607955
Biobank	rs267607955
1000 genomes	rs267607955
hgdp	rs267607955
ensembl	rs267607955
geneview	rs267607955
scholar	rs267607955
google	rs267607955
pharmgkb	rs267607955
gwascentral	rs267607955
openSNP	rs267607955
23andMe	rs267607955
SNPshot	rs267607955
SNPdbe	rs267607955
MSV3d	rs267607955
GWAS Ctlg	rs267607955

Max Magnitude

6

ClinVar
Risk	rs267607955(-;-)
Alt	rs267607955(-;-)
Reference	Rs267607955(AAGT;AAGT)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47672755_47672758delAAGT
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076129.2,