rs267607928

Orientation

plus

Stabilized

plus

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

Make rs267607928(-;-)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47410278

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs267607928
dbSNP (classic)	rs267607928
ClinGen	rs267607928
ebi	rs267607928
HLI	rs267607928
Exac	rs267607928
Gnomad	rs267607928
Varsome	rs267607928
LitVar	rs267607928
Map	rs267607928
PheGenI	rs267607928
Biobank	rs267607928
1000 genomes	rs267607928
hgdp	rs267607928
ensembl	rs267607928
geneview	rs267607928
scholar	rs267607928
google	rs267607928
pharmgkb	rs267607928
gwascentral	rs267607928
openSNP	rs267607928
23andMe	rs267607928
SNPshot	rs267607928
SNPdbe	rs267607928
MSV3d	rs267607928
GWAS Ctlg	rs267607928

Max Magnitude

6

ClinVar
Risk	rs267607928(-;-)
Alt	rs267607928(-;-)
Reference	Rs267607928(T;T)
Significance	Pathogenic
Disease	Lynch syndrome not provided
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome not provided
Reversed	0
HGVS	NC_000002.11:g.47637417delT
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076636.2, RCV000481227.1,