rs267608041

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;A)	6	Lynch syndrome
(A;A)	0	common in clinvar

Make rs267608041(-;-)

Reference

GRCh38.p2 38.2/147

Chromosome

2

Position

47798724

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs267608041
dbSNP (classic)	rs267608041
ClinGen	rs267608041
ebi	rs267608041
HLI	rs267608041
Exac	rs267608041
Gnomad	rs267608041
Varsome	rs267608041
LitVar	rs267608041
Map	rs267608041
PheGenI	rs267608041
Biobank	rs267608041
1000 genomes	rs267608041
hgdp	rs267608041
ensembl	rs267608041
geneview	rs267608041
scholar	rs267608041
google	rs267608041
pharmgkb	rs267608041
gwascentral	rs267608041
openSNP	rs267608041
23andMe	rs267608041
SNPshot	rs267608041
SNPdbe	rs267608041
MSV3d	rs267608041
GWAS Ctlg	rs267608041

Max Magnitude

6

ClinVar
Risk	rs267608041(-;-)
Alt	rs267608041(-;-)
Reference	Rs267608041(A;A)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH6
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.48025863delA
CLNSRC
CLNACC	RCV000231668.1,