rs267608084

Orientation

plus

Stabilized

plus

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

Make rs267608084(T;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47803602

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs267608084
dbSNP (classic)	rs267608084
ClinGen	rs267608084
ebi	rs267608084
HLI	rs267608084
Exac	rs267608084
Gnomad	rs267608084
Varsome	rs267608084
LitVar	rs267608084
Map	rs267608084
PheGenI	rs267608084
Biobank	rs267608084
1000 genomes	rs267608084
hgdp	rs267608084
ensembl	rs267608084
geneview	rs267608084
scholar	rs267608084
google	rs267608084
pharmgkb	rs267608084
gwascentral	rs267608084
openSNP	rs267608084
23andMe	rs267608084
SNPshot	rs267608084
SNPdbe	rs267608084
MSV3d	rs267608084
GWAS Ctlg	rs267608084

Max Magnitude

6

c.3355G>T (p.Glu1119Ter)

23andMe name: i5046092

ClinVar
Risk	rs267608084(A;A) rs267608084(T;T)
Alt	rs267608084(A;A) rs267608084(T;T)
Reference	Rs267608084(G;G)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome Lynch syndrome
Variation	info
Gene	MSH6
CLNDBN	Hereditary cancer-predisposing syndrome Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.48030741G>A; NC_000002.11:g.48030741G>T
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000491737.1, RCV000074842.2,