rs267607742

Orientation

plus

Stabilized

plus

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

Make rs267607742(A;A)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37004476

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs267607742
dbSNP (classic)	rs267607742
ClinGen	rs267607742
ebi	rs267607742
HLI	rs267607742
Exac	rs267607742
Gnomad	rs267607742
Varsome	rs267607742
LitVar	rs267607742
Map	rs267607742
PheGenI	rs267607742
Biobank	rs267607742
1000 genomes	rs267607742
hgdp	rs267607742
ensembl	rs267607742
geneview	rs267607742
scholar	rs267607742
google	rs267607742
pharmgkb	rs267607742
gwascentral	rs267607742
openSNP	rs267607742
23andMe	rs267607742
SNPshot	rs267607742
SNPdbe	rs267607742
MSV3d	rs267607742
GWAS Ctlg	rs267607742

Max Magnitude

6

ClinVar
Risk	rs267607742(A;A) rs267607742(C;C)
Alt	rs267607742(A;A) rs267607742(C;C)
Reference	Rs267607742(T;T)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37045967T>A; NC_000003.11:g.37045967T>C
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075680.2, RCV000075681.2,