rs267608055

Orientation

plus

Stabilized

plus

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

Make rs267608055(A;A)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47799282

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs267608055
dbSNP (classic)	rs267608055
ClinGen	rs267608055
ebi	rs267608055
HLI	rs267608055
Exac	rs267608055
Gnomad	rs267608055
Varsome	rs267608055
LitVar	rs267608055
Map	rs267608055
PheGenI	rs267608055
Biobank	rs267608055
1000 genomes	rs267608055
hgdp	rs267608055
ensembl	rs267608055
geneview	rs267608055
scholar	rs267608055
google	rs267608055
pharmgkb	rs267608055
gwascentral	rs267608055
openSNP	rs267608055
23andMe	rs267608055
SNPshot	rs267608055
SNPdbe	rs267608055
MSV3d	rs267608055
GWAS Ctlg	rs267608055

Max Magnitude

6

c.1299T>A (p.Tyr433Ter)

23andMe name: i5046109

ClinVar
Risk	rs267608055(A;A) rs267608055(G;G)
Alt	rs267608055(A;A) rs267608055(G;G)
Reference	Rs267608055(T;T)
Significance	Pathogenic
Disease	Lynch syndrome Hereditary cancer-predisposing syndrome
Variation	info
Gene	MSH6
CLNDBN	Lynch syndrome Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000002.11:g.48026421T>A; NC_000002.11:g.48026421T>G
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000074647.2, RCV000491745.1,