rs267607915

Orientation

plus

Stabilized

plus

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

Make rs267607915(-;-)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47403211

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs267607915
dbSNP (classic)	rs267607915
ClinGen	rs267607915
ebi	rs267607915
HLI	rs267607915
Exac	rs267607915
Gnomad	rs267607915
Varsome	rs267607915
LitVar	rs267607915
Map	rs267607915
PheGenI	rs267607915
Biobank	rs267607915
1000 genomes	rs267607915
hgdp	rs267607915
ensembl	rs267607915
geneview	rs267607915
scholar	rs267607915
google	rs267607915
pharmgkb	rs267607915
gwascentral	rs267607915
openSNP	rs267607915
23andMe	rs267607915
SNPshot	rs267607915
SNPdbe	rs267607915
MSV3d	rs267607915
GWAS Ctlg	rs267607915

Max Magnitude

6

ClinVar
Risk	rs267607915(-;-)
Alt	rs267607915(-;-)
Reference	Rs267607915(A;A)
Significance	Pathogenic
Disease	Lynch syndrome not provided Hereditary cancer-predisposing syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome not provided Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000002.11:g.47630350delA
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076388.2, RCV000202031.1, RCV000218615.2,