rs267607825

Orientation

minus

Stabilized

minus

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

Make rs267607825(T;T)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37026008

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs267607825
dbSNP (classic)	rs267607825
ClinGen	rs267607825
ebi	rs267607825
HLI	rs267607825
Exac	rs267607825
Gnomad	rs267607825
Varsome	rs267607825
LitVar	rs267607825
Map	rs267607825
PheGenI	rs267607825
Biobank	rs267607825
1000 genomes	rs267607825
hgdp	rs267607825
ensembl	rs267607825
geneview	rs267607825
scholar	rs267607825
google	rs267607825
pharmgkb	rs267607825
gwascentral	rs267607825
openSNP	rs267607825
23andMe	rs267607825
SNPshot	rs267607825
SNPdbe	rs267607825
MSV3d	rs267607825
GWAS Ctlg	rs267607825

Max Magnitude

6

ClinVar
Risk	rs267607825(A;A) rs267607825(G;G) rs267607825(T;T)
Alt	rs267607825(A;A) rs267607825(G;G) rs267607825(T;T)
Reference	Rs267607825(C;C)
Significance	Pathogenic
Disease	Lynch syndrome Hereditary cancer-predisposing syndrome not provided
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome Hereditary cancer-predisposing syndrome not provided
Reversed	1
HGVS	NC_000003.11:g.37067499G>A; NC_000003.11:g.37067499G>C; NC_000003.11:g.37067499G>T
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075192.2, RCV000220831.1, RCV000075193.2, RCV000482715.1,