rs267608062

Orientation

plus

Stabilized

plus

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

Reference

GRCh38 38.1/141

Chromosome

2

Position

47798828

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs267608062
dbSNP (classic)	rs267608062
ClinGen	rs267608062
ebi	rs267608062
HLI	rs267608062
Exac	rs267608062
Gnomad	rs267608062
Varsome	rs267608062
LitVar	rs267608062
Map	rs267608062
PheGenI	rs267608062
Biobank	rs267608062
1000 genomes	rs267608062
hgdp	rs267608062
ensembl	rs267608062
geneview	rs267608062
scholar	rs267608062
google	rs267608062
pharmgkb	rs267608062
gwascentral	rs267608062
openSNP	rs267608062
23andMe	rs267608062
SNPshot	rs267608062
SNPdbe	rs267608062
MSV3d	rs267608062
GWAS Ctlg	rs267608062

Max Magnitude

6

ClinVar
Risk	rs267608062(GGG;GGG) Rs267608062(T;T)
Alt	rs267608062(GGG;GGG) Rs267608062(T;T)
Reference	Rs267608062(-;-)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH6
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.48025967dupT
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075039.2,