rs267607801

Orientation

plus

Stabilized

plus

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

Make rs267607801(-;-)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37017523

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs267607801
dbSNP (classic)	rs267607801
ClinGen	rs267607801
ebi	rs267607801
HLI	rs267607801
Exac	rs267607801
Gnomad	rs267607801
Varsome	rs267607801
LitVar	rs267607801
Map	rs267607801
PheGenI	rs267607801
Biobank	rs267607801
1000 genomes	rs267607801
hgdp	rs267607801
ensembl	rs267607801
geneview	rs267607801
scholar	rs267607801
google	rs267607801
pharmgkb	rs267607801
gwascentral	rs267607801
openSNP	rs267607801
23andMe	rs267607801
SNPshot	rs267607801
SNPdbe	rs267607801
MSV3d	rs267607801
GWAS Ctlg	rs267607801

Max Magnitude

6

ClinVar
Risk	rs267607801(-;-)
Alt	rs267607801(-;-)
Reference	Rs267607801(ACTT;ACTT)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37059014_37059017delACTT
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075876.2,