rs267607809

Orientation

plus

Stabilized

plus

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

Make rs267607809(-;-)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37020313

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs267607809
dbSNP (classic)	rs267607809
ClinGen	rs267607809
ebi	rs267607809
HLI	rs267607809
Exac	rs267607809
Gnomad	rs267607809
Varsome	rs267607809
LitVar	rs267607809
Map	rs267607809
PheGenI	rs267607809
Biobank	rs267607809
1000 genomes	rs267607809
hgdp	rs267607809
ensembl	rs267607809
geneview	rs267607809
scholar	rs267607809
google	rs267607809
pharmgkb	rs267607809
gwascentral	rs267607809
openSNP	rs267607809
23andMe	rs267607809
SNPshot	rs267607809
SNPdbe	rs267607809
MSV3d	rs267607809
GWAS Ctlg	rs267607809

Max Magnitude

6

ClinVar
Risk	rs267607809(-;-)
Alt	rs267607809(-;-)
Reference	Rs267607809(A;A)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37061804delA
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075925.2,