rs267608106

Orientation

plus

Stabilized

plus

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

Make rs267608106(-;-)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47805707

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs267608106
dbSNP (classic)	rs267608106
ClinGen	rs267608106
ebi	rs267608106
HLI	rs267608106
Exac	rs267608106
Gnomad	rs267608106
Varsome	rs267608106
LitVar	rs267608106
Map	rs267608106
PheGenI	rs267608106
Biobank	rs267608106
1000 genomes	rs267608106
hgdp	rs267608106
ensembl	rs267608106
geneview	rs267608106
scholar	rs267608106
google	rs267608106
pharmgkb	rs267608106
gwascentral	rs267608106
openSNP	rs267608106
23andMe	rs267608106
SNPshot	rs267608106
SNPdbe	rs267608106
MSV3d	rs267608106
GWAS Ctlg	rs267608106

Max Magnitude

6

\

c.3646_3646+3del

23andMe name: i5037879

ClinVar
Risk	rs267608106(-;-)
Alt	rs267608106(-;-)
Reference	Rs267608106(TAGG;TAGG)
Significance	Probable-Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH6
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.48032846_48032849delGGTA
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000074901.3,