rs267607754

Orientation

plus

Stabilized

plus

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

Make rs267607754(-;-)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37008848

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs267607754
dbSNP (classic)	rs267607754
ClinGen	rs267607754
ebi	rs267607754
HLI	rs267607754
Exac	rs267607754
Gnomad	rs267607754
Varsome	rs267607754
LitVar	rs267607754
Map	rs267607754
PheGenI	rs267607754
Biobank	rs267607754
1000 genomes	rs267607754
hgdp	rs267607754
ensembl	rs267607754
geneview	rs267607754
scholar	rs267607754
google	rs267607754
pharmgkb	rs267607754
gwascentral	rs267607754
openSNP	rs267607754
23andMe	rs267607754
SNPshot	rs267607754
SNPdbe	rs267607754
MSV3d	rs267607754
GWAS Ctlg	rs267607754

Max Magnitude

6

ClinVar
Risk	rs267607754(-;-)
Alt	rs267607754(-;-)
Reference	Rs267607754(G;G)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37050339delG
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075734.2,