rs267608083

Orientation

plus

Stabilized

plus

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

Make rs267608083(A;A)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

47800062

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs267608083
dbSNP (classic)	rs267608083
ClinGen	rs267608083
ebi	rs267608083
HLI	rs267608083
Exac	rs267608083
Gnomad	rs267608083
Varsome	rs267608083
LitVar	rs267608083
Map	rs267608083
PheGenI	rs267608083
Biobank	rs267608083
1000 genomes	rs267608083
hgdp	rs267608083
ensembl	rs267608083
geneview	rs267608083
scholar	rs267608083
google	rs267608083
pharmgkb	rs267608083
gwascentral	rs267608083
openSNP	rs267608083
23andMe	rs267608083
SNPshot	rs267608083
SNPdbe	rs267608083
MSV3d	rs267608083
GWAS Ctlg	rs267608083

Max Magnitude

6

ClinVar
Risk	rs267608083(A;A)
Alt	rs267608083(A;A)
Reference	Rs267608083(-;-)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome Lynch syndrome
Variation	info
Gene	MSH6
CLNDBN	Hereditary cancer-predisposing syndrome Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.48027201dupA
CLNSRC
CLNACC	RCV000167251.2, RCV000210176.1,