rs267608086

Orientation

plus

Stabilized

plus

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

Make rs267608086(T;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47803614

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs267608086
dbSNP (classic)	rs267608086
ClinGen	rs267608086
ebi	rs267608086
HLI	rs267608086
Exac	rs267608086
Gnomad	rs267608086
Varsome	rs267608086
LitVar	rs267608086
Map	rs267608086
PheGenI	rs267608086
Biobank	rs267608086
1000 genomes	rs267608086
hgdp	rs267608086
ensembl	rs267608086
geneview	rs267608086
scholar	rs267608086
google	rs267608086
pharmgkb	rs267608086
gwascentral	rs267608086
openSNP	rs267608086
23andMe	rs267608086
SNPshot	rs267608086
SNPdbe	rs267608086
MSV3d	rs267608086
GWAS Ctlg	rs267608086

Max Magnitude

6

ClinVar
Risk	rs267608086(T;T)
Alt	rs267608086(T;T)
Reference	Rs267608086(G;G)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH6
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.48030753G>T
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000074843.2,