rs267608085

Orientation

plus

Stabilized

plus

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

Make rs267608085(-;-)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47803442

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs267608085
dbSNP (classic)	rs267608085
ClinGen	rs267608085
ebi	rs267608085
HLI	rs267608085
Exac	rs267608085
Gnomad	rs267608085
Varsome	rs267608085
LitVar	rs267608085
Map	rs267608085
PheGenI	rs267608085
Biobank	rs267608085
1000 genomes	rs267608085
hgdp	rs267608085
ensembl	rs267608085
geneview	rs267608085
scholar	rs267608085
google	rs267608085
pharmgkb	rs267608085
gwascentral	rs267608085
openSNP	rs267608085
23andMe	rs267608085
SNPshot	rs267608085
SNPdbe	rs267608085
MSV3d	rs267608085
GWAS Ctlg	rs267608085

Max Magnitude

6

c.3195_3198delCTAT (p.Asn1065Lysfs)

23andMe name: i5037877

ClinVar
Risk	rs267608085(-;-)
Alt	rs267608085(-;-)
Reference	Rs267608085(CTAT;CTAT)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH6
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.48030581_48030584delCTAT
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000074815.2,