rs267607783

Orientation

plus

Stabilized

plus

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

Make rs267607783(-;-)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37014429

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs267607783
dbSNP (classic)	rs267607783
ClinGen	rs267607783
ebi	rs267607783
HLI	rs267607783
Exac	rs267607783
Gnomad	rs267607783
Varsome	rs267607783
LitVar	rs267607783
Map	rs267607783
PheGenI	rs267607783
Biobank	rs267607783
1000 genomes	rs267607783
hgdp	rs267607783
ensembl	rs267607783
geneview	rs267607783
scholar	rs267607783
google	rs267607783
pharmgkb	rs267607783
gwascentral	rs267607783
openSNP	rs267607783
23andMe	rs267607783
SNPshot	rs267607783
SNPdbe	rs267607783
MSV3d	rs267607783
GWAS Ctlg	rs267607783

Max Magnitude

6

ClinVar
Risk	rs267607783(-;-)
Alt	rs267607783(-;-)
Reference	Rs267607783(AT;AT)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37055920_37055921delTA
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075817.2,