rs267608035

Orientation

plus

Stabilized

plus

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

Make rs267608035(A;A)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47795893

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs267608035
dbSNP (classic)	rs267608035
ClinGen	rs267608035
ebi	rs267608035
HLI	rs267608035
Exac	rs267608035
Gnomad	rs267608035
Varsome	rs267608035
LitVar	rs267608035
Map	rs267608035
PheGenI	rs267608035
Biobank	rs267608035
1000 genomes	rs267608035
hgdp	rs267608035
ensembl	rs267608035
geneview	rs267608035
scholar	rs267608035
google	rs267608035
pharmgkb	rs267608035
gwascentral	rs267608035
openSNP	rs267608035
23andMe	rs267608035
SNPshot	rs267608035
SNPdbe	rs267608035
MSV3d	rs267608035
GWAS Ctlg	rs267608035

Max Magnitude

6

ClinVar
Risk	rs267608035(A;A)
Alt	rs267608035(A;A)
Reference	Rs267608035(G;G)
Significance	Probable-Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH6
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.48023032G>A
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075000.2,