rs267607889

Orientation

plus

Stabilized

plus

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

Make rs267607889(T;T)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37050484

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs267607889
dbSNP (old)	rs267607889
ClinGen	rs267607889
ebi	rs267607889
HLI	rs267607889
Exac	rs267607889
Gnomad	rs267607889
Varsome	rs267607889
LitVar	rs267607889
Map	rs267607889
PheGenI	rs267607889
Biobank	rs267607889
1000 genomes	rs267607889
hgdp	rs267607889
ensembl	rs267607889
gopubmed	rs267607889
geneview	rs267607889
scholar	rs267607889
google	rs267607889
pharmgkb	rs267607889
gwascentral	rs267607889
openSNP	rs267607889
23andMe	rs267607889
23andMe all	rs267607889
SNPshot	rs267607889
SNPdbe	rs267607889
MSV3d	rs267607889
GWAS Ctlg	rs267607889

Max Magnitude

6

ClinVar
Risk	rs267607889(G;G) rs267607889(T;T)
Alt	rs267607889(G;G) rs267607889(T;T)
Reference	Rs267607889(A;A)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37091975A>G; NC_000003.11:g.37091975A>T
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075539.2, RCV000075540.2,