rs267607837

Orientation

plus

Stabilized

plus

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

Make rs267607837(A;A)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37040185

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs267607837
dbSNP (classic)	rs267607837
ClinGen	rs267607837
ebi	rs267607837
HLI	rs267607837
Exac	rs267607837
Gnomad	rs267607837
Varsome	rs267607837
LitVar	rs267607837
Map	rs267607837
PheGenI	rs267607837
Biobank	rs267607837
1000 genomes	rs267607837
hgdp	rs267607837
ensembl	rs267607837
geneview	rs267607837
scholar	rs267607837
google	rs267607837
pharmgkb	rs267607837
gwascentral	rs267607837
openSNP	rs267607837
23andMe	rs267607837
SNPshot	rs267607837
SNPdbe	rs267607837
MSV3d	rs267607837
GWAS Ctlg	rs267607837

Max Magnitude

6

ClinVar
Risk	rs267607837(A;A) rs267607837(C;C) rs267607837(T;T)
Alt	rs267607837(A;A) rs267607837(C;C) rs267607837(T;T)
Reference	Rs267607837(G;G)
Significance	Pathogenic
Disease	Lynch syndrome not provided
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome not provided
Reversed	0
HGVS	NC_000003.11:g.37081676G>A; NC_000003.11:g.37081676G>C; NC_000003.11:g.37081676G>T
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075253.2, RCV000075254.2, RCV000075255.2, RCV000485205.1,