rs267608112

Orientation

plus

Stabilized

plus

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

Make rs267608112(-;-)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47806198

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs267608112
dbSNP (classic)	rs267608112
ClinGen	rs267608112
ebi	rs267608112
HLI	rs267608112
Exac	rs267608112
Gnomad	rs267608112
Varsome	rs267608112
LitVar	rs267608112
Map	rs267608112
PheGenI	rs267608112
Biobank	rs267608112
1000 genomes	rs267608112
hgdp	rs267608112
ensembl	rs267608112
geneview	rs267608112
scholar	rs267608112
google	rs267608112
pharmgkb	rs267608112
gwascentral	rs267608112
openSNP	rs267608112
23andMe	rs267608112
SNPshot	rs267608112
SNPdbe	rs267608112
MSV3d	rs267608112
GWAS Ctlg	rs267608112

Max Magnitude

6

ClinVar
Risk	rs267608112(-;-)
Alt	rs267608112(-;-)
Reference	Rs267608112(TAACAG;TAACAG)
Significance	Probable-Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH6
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.48033337_48033342delTAACAG
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000074908.2,