rs267607798

Orientation

plus

Stabilized

plus

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

Make rs267607798(-;-)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37014545

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs267607798
dbSNP (classic)	rs267607798
ClinGen	rs267607798
ebi	rs267607798
HLI	rs267607798
Exac	rs267607798
Gnomad	rs267607798
Varsome	rs267607798
LitVar	rs267607798
Map	rs267607798
PheGenI	rs267607798
Biobank	rs267607798
1000 genomes	rs267607798
hgdp	rs267607798
ensembl	rs267607798
geneview	rs267607798
scholar	rs267607798
google	rs267607798
pharmgkb	rs267607798
gwascentral	rs267607798
openSNP	rs267607798
23andMe	rs267607798
SNPshot	rs267607798
SNPdbe	rs267607798
MSV3d	rs267607798
GWAS Ctlg	rs267607798

Max Magnitude

6

ClinVar
Risk	rs267607798(-;-)
Alt	rs267607798(-;-)
Reference	Rs267607798(G;G)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37056036delG
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075849.2,