rs267607779

Orientation

plus

Stabilized

plus

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

Make rs267607779(-;-)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37012100

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs267607779
dbSNP (classic)	rs267607779
ClinGen	rs267607779
ebi	rs267607779
HLI	rs267607779
Exac	rs267607779
Gnomad	rs267607779
Varsome	rs267607779
LitVar	rs267607779
Map	rs267607779
PheGenI	rs267607779
Biobank	rs267607779
1000 genomes	rs267607779
hgdp	rs267607779
ensembl	rs267607779
geneview	rs267607779
scholar	rs267607779
google	rs267607779
pharmgkb	rs267607779
gwascentral	rs267607779
openSNP	rs267607779
23andMe	rs267607779
SNPshot	rs267607779
SNPdbe	rs267607779
MSV3d	rs267607779
GWAS Ctlg	rs267607779

Max Magnitude

6

ClinVar
Risk	rs267607779(-;-)
Alt	rs267607779(-;-)
Reference	Rs267607779(G;G)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37053591delG
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075804.2,