rs267607884

Orientation

minus

Stabilized

minus

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

Make rs267607884(T;T)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37048903

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs267607884
dbSNP (classic)	rs267607884
ClinGen	rs267607884
ebi	rs267607884
HLI	rs267607884
Exac	rs267607884
Gnomad	rs267607884
Varsome	rs267607884
LitVar	rs267607884
Map	rs267607884
PheGenI	rs267607884
Biobank	rs267607884
1000 genomes	rs267607884
hgdp	rs267607884
ensembl	rs267607884
geneview	rs267607884
scholar	rs267607884
google	rs267607884
pharmgkb	rs267607884
gwascentral	rs267607884
openSNP	rs267607884
23andMe	rs267607884
SNPshot	rs267607884
SNPdbe	rs267607884
MSV3d	rs267607884
GWAS Ctlg	rs267607884

Max Magnitude

6

ClinVar
Risk	rs267607884(A;A) rs267607884(T;T)
Alt	rs267607884(A;A) rs267607884(T;T)
Reference	Rs267607884(C;C)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	1
HGVS	NC_000003.11:g.37090394G>A; NC_000003.11:g.37090394G>T
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075467.2, RCV000075468.2,