rs267608058

Orientation

plus

Stabilized

plus

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

Make rs267608058(-;-)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47800133

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs267608058
dbSNP (classic)	rs267608058
ClinGen	rs267608058
ebi	rs267608058
HLI	rs267608058
Exac	rs267608058
Gnomad	rs267608058
Varsome	rs267608058
LitVar	rs267608058
Map	rs267608058
PheGenI	rs267608058
Biobank	rs267608058
1000 genomes	rs267608058
hgdp	rs267608058
ensembl	rs267608058
geneview	rs267608058
scholar	rs267608058
google	rs267608058
pharmgkb	rs267608058
gwascentral	rs267608058
openSNP	rs267608058
23andMe	rs267608058
SNPshot	rs267608058
SNPdbe	rs267608058
MSV3d	rs267608058
GWAS Ctlg	rs267608058

Merged from

Rs587782275

Max Magnitude

6

ClinVar
Risk	rs267608058(-;-) Rs267608058(CAGT;CAGT)
Alt	rs267608058(-;-) Rs267608058(CAGT;CAGT)
Reference	Rs267608058(TCAG;TCAG)
Significance	Pathogenic
Disease	Lynch syndrome Hereditary cancer-predisposing syndrome not provided Hereditary nonpolyposis colorectal cancer type 5
Variation	info
Gene	MSH6
CLNDBN	Lynch syndrome Hereditary cancer-predisposing syndrome not provided Hereditary nonpolyposis colorectal cancer type 5
Reversed	0
HGVS	NC_000002.11:g.48027272_48027275delTCAG
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000074720.2, RCV000162408.3, RCV000202111.3, RCV000411212.1,