rs267608076

Orientation

plus

Stabilized

plus

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

Make rs267608076(-;-)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47799620

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs267608076
dbSNP (classic)	rs267608076
ClinGen	rs267608076
ebi	rs267608076
HLI	rs267608076
Exac	rs267608076
Gnomad	rs267608076
Varsome	rs267608076
LitVar	rs267608076
Map	rs267608076
PheGenI	rs267608076
Biobank	rs267608076
1000 genomes	rs267608076
hgdp	rs267608076
ensembl	rs267608076
geneview	rs267608076
scholar	rs267608076
google	rs267608076
pharmgkb	rs267608076
gwascentral	rs267608076
openSNP	rs267608076
23andMe	rs267608076
SNPshot	rs267608076
SNPdbe	rs267608076
MSV3d	rs267608076
GWAS Ctlg	rs267608076

Max Magnitude

6

ClinVar
Risk	rs267608076(-;-)
Alt	rs267608076(-;-)
Reference	Rs267608076(AG;AG)
Significance	Pathogenic
Disease	Lynch syndrome not provided
Variation	info
Gene	MSH6
CLNDBN	Lynch syndrome not provided
Reversed	0
HGVS	NC_000002.11:g.48026759_48026760delAG
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000074676.2, RCV000217244.1,