rs267607696

Orientation

plus

Stabilized

plus

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

Make rs267607696(GG;GG)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47445611

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs267607696
dbSNP (classic)	rs267607696
ClinGen	rs267607696
ebi	rs267607696
HLI	rs267607696
Exac	rs267607696
Gnomad	rs267607696
Varsome	rs267607696
LitVar	rs267607696
Map	rs267607696
PheGenI	rs267607696
Biobank	rs267607696
1000 genomes	rs267607696
hgdp	rs267607696
ensembl	rs267607696
geneview	rs267607696
scholar	rs267607696
google	rs267607696
pharmgkb	rs267607696
gwascentral	rs267607696
openSNP	rs267607696
23andMe	rs267607696
SNPshot	rs267607696
SNPdbe	rs267607696
MSV3d	rs267607696
GWAS Ctlg	rs267607696

Max Magnitude

6

ClinVar
Risk	rs267607696(GG;GG)
Alt	rs267607696(GG;GG)
Reference	Rs267607696(-;-)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47672750_47672751insGG
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076127.2,