rs267607787

Orientation

plus

Stabilized

plus

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

Make rs267607787(-;-)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37014481

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs267607787
dbSNP (classic)	rs267607787
ClinGen	rs267607787
ebi	rs267607787
HLI	rs267607787
Exac	rs267607787
Gnomad	rs267607787
Varsome	rs267607787
LitVar	rs267607787
Map	rs267607787
PheGenI	rs267607787
Biobank	rs267607787
1000 genomes	rs267607787
hgdp	rs267607787
ensembl	rs267607787
geneview	rs267607787
scholar	rs267607787
google	rs267607787
pharmgkb	rs267607787
gwascentral	rs267607787
openSNP	rs267607787
23andMe	rs267607787
SNPshot	rs267607787
SNPdbe	rs267607787
MSV3d	rs267607787
GWAS Ctlg	rs267607787

Max Magnitude

6

ClinVar
Risk	rs267607787(-;-)
Alt	rs267607787(-;-)
Reference	Rs267607787(AATG;AATG)
Significance	Pathogenic
Disease	Lynch syndrome Hereditary cancer-predisposing syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000003.11:g.37055972_37055975delAATG
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075829.2, RCV000220921.1,