rs267607759

Orientation

plus

Stabilized

plus

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

Make rs267607759(G;G)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37011818

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs267607759
dbSNP (classic)	rs267607759
ClinGen	rs267607759
ebi	rs267607759
HLI	rs267607759
Exac	rs267607759
Gnomad	rs267607759
Varsome	rs267607759
LitVar	rs267607759
Map	rs267607759
PheGenI	rs267607759
Biobank	rs267607759
1000 genomes	rs267607759
hgdp	rs267607759
ensembl	rs267607759
geneview	rs267607759
scholar	rs267607759
google	rs267607759
pharmgkb	rs267607759
gwascentral	rs267607759
openSNP	rs267607759
23andMe	rs267607759
SNPshot	rs267607759
SNPdbe	rs267607759
MSV3d	rs267607759
GWAS Ctlg	rs267607759

Max Magnitude

6

ClinVar
Risk	rs267607759(C;C) rs267607759(G;G)
Alt	rs267607759(C;C) rs267607759(G;G)
Reference	Rs267607759(A;A)
Significance	Pathogenic
Disease	Lynch syndrome not provided
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome not provided
Reversed	0
HGVS	NC_000003.11:g.37053309A>C; NC_000003.11:g.37053309A>G
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075755.2, RCV000075756.2, RCV000202027.1,