rs267608096

Orientation

plus

Stabilized

plus

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

Make rs267608096(A;A)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47803686

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs267608096
dbSNP (classic)	rs267608096
ClinGen	rs267608096
ebi	rs267608096
HLI	rs267608096
Exac	rs267608096
Gnomad	rs267608096
Varsome	rs267608096
LitVar	rs267608096
Map	rs267608096
PheGenI	rs267608096
Biobank	rs267608096
1000 genomes	rs267608096
hgdp	rs267608096
ensembl	rs267608096
geneview	rs267608096
scholar	rs267608096
google	rs267608096
pharmgkb	rs267608096
gwascentral	rs267608096
openSNP	rs267608096
23andMe	rs267608096
SNPshot	rs267608096
SNPdbe	rs267608096
MSV3d	rs267608096
GWAS Ctlg	rs267608096

Max Magnitude

6

ClinVar
Risk	rs267608096(A;A)
Alt	rs267608096(A;A)
Reference	Rs267608096(G;G)
Significance	Probable-Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH6
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.48030825G>A
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000074854.2,