rs267608114

Orientation

plus

Stabilized

plus

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

Make rs267608114(-;-)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47806356

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs267608114
dbSNP (classic)	rs267608114
ClinGen	rs267608114
ebi	rs267608114
HLI	rs267608114
Exac	rs267608114
Gnomad	rs267608114
Varsome	rs267608114
LitVar	rs267608114
Map	rs267608114
PheGenI	rs267608114
Biobank	rs267608114
1000 genomes	rs267608114
hgdp	rs267608114
ensembl	rs267608114
geneview	rs267608114
scholar	rs267608114
google	rs267608114
pharmgkb	rs267608114
gwascentral	rs267608114
openSNP	rs267608114
23andMe	rs267608114
SNPshot	rs267608114
SNPdbe	rs267608114
MSV3d	rs267608114
GWAS Ctlg	rs267608114

Max Magnitude

6

c.3799_3800delAT (p.Met1267Glyfs)

23andMe name: i5037866

ClinVar
Risk	rs267608114(-;-)
Alt	rs267608114(-;-)
Reference	Rs267608114(AT;AT)
Significance	Pathogenic
Disease	Lynch syndrome not provided Hereditary cancer-predisposing syndrome
Variation	info
Gene	MSH6
CLNDBN	Lynch syndrome not provided Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000002.11:g.48033495_48033496delAT
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000074931.2, RCV000202066.1, RCV000491355.1,