rs267607739

Orientation

plus

Stabilized

plus

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

Make rs267607739(A;A)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37004440

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs267607739
dbSNP (classic)	rs267607739
ClinGen	rs267607739
ebi	rs267607739
HLI	rs267607739
Exac	rs267607739
Gnomad	rs267607739
Varsome	rs267607739
LitVar	rs267607739
Map	rs267607739
PheGenI	rs267607739
Biobank	rs267607739
1000 genomes	rs267607739
hgdp	rs267607739
ensembl	rs267607739
geneview	rs267607739
scholar	rs267607739
google	rs267607739
pharmgkb	rs267607739
gwascentral	rs267607739
openSNP	rs267607739
23andMe	rs267607739
SNPshot	rs267607739
SNPdbe	rs267607739
MSV3d	rs267607739
GWAS Ctlg	rs267607739

Max Magnitude

6

ClinVar
Risk	rs267607739(A;A)
Alt	rs267607739(A;A)
Reference	Rs267607739(-;-)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37045931dupA
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075662.2,