rs267607877

Orientation

plus

Stabilized

plus

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

Make rs267607877(-;-)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37048608

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs267607877
dbSNP (classic)	rs267607877
ClinGen	rs267607877
ebi	rs267607877
HLI	rs267607877
Exac	rs267607877
Gnomad	rs267607877
Varsome	rs267607877
LitVar	rs267607877
Map	rs267607877
PheGenI	rs267607877
Biobank	rs267607877
1000 genomes	rs267607877
hgdp	rs267607877
ensembl	rs267607877
geneview	rs267607877
scholar	rs267607877
google	rs267607877
pharmgkb	rs267607877
gwascentral	rs267607877
openSNP	rs267607877
23andMe	rs267607877
SNPshot	rs267607877
SNPdbe	rs267607877
MSV3d	rs267607877
GWAS Ctlg	rs267607877

Max Magnitude

6

ClinVar
Risk	rs267607877(-;-)
Alt	rs267607877(-;-)
Reference	Rs267607877(A;A)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37090099delA
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075454.2,