rs267608082

Orientation

plus

Stabilized

plus

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

Make rs267608082(-;-)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47799884

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs267608082
dbSNP (classic)	rs267608082
ClinGen	rs267608082
ebi	rs267608082
HLI	rs267608082
Exac	rs267608082
Gnomad	rs267608082
Varsome	rs267608082
LitVar	rs267608082
Map	rs267608082
PheGenI	rs267608082
Biobank	rs267608082
1000 genomes	rs267608082
hgdp	rs267608082
ensembl	rs267608082
geneview	rs267608082
scholar	rs267608082
google	rs267608082
pharmgkb	rs267608082
gwascentral	rs267608082
openSNP	rs267608082
23andMe	rs267608082
SNPshot	rs267608082
SNPdbe	rs267608082
MSV3d	rs267608082
GWAS Ctlg	rs267608082

Max Magnitude

6

ClinVar
Risk	rs267608082(-;-)
Alt	rs267608082(-;-)
Reference	Rs267608082(TG;TG)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH6
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.48027023_48027024delTG
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000074696.2,