rs267608091

Orientation

plus

Stabilized

plus

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

Make rs267608091(T;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47803510

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs267608091
dbSNP (classic)	rs267608091
ClinGen	rs267608091
ebi	rs267608091
HLI	rs267608091
Exac	rs267608091
Gnomad	rs267608091
Varsome	rs267608091
LitVar	rs267608091
Map	rs267608091
PheGenI	rs267608091
Biobank	rs267608091
1000 genomes	rs267608091
hgdp	rs267608091
ensembl	rs267608091
geneview	rs267608091
scholar	rs267608091
google	rs267608091
pharmgkb	rs267608091
gwascentral	rs267608091
openSNP	rs267608091
23andMe	rs267608091
SNPshot	rs267608091
SNPdbe	rs267608091
MSV3d	rs267608091
GWAS Ctlg	rs267608091

Max Magnitude

6

ClinVar
Risk	rs267608091(T;T)
Alt	rs267608091(T;T)
Reference	Rs267608091(-;-)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH6
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.48030649dupT
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000074832.2,