rs267607738

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;-)	0	common in clinvar
(-;T)	6	Lynch syndrome, pathogenic mutation
(D;D)	0	common genotype

Make rs267607738(T;T)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37001055

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs267607738
dbSNP (classic)	rs267607738
ClinGen	rs267607738
ebi	rs267607738
HLI	rs267607738
Exac	rs267607738
Gnomad	rs267607738
Varsome	rs267607738
LitVar	rs267607738
Map	rs267607738
PheGenI	rs267607738
Biobank	rs267607738
1000 genomes	rs267607738
hgdp	rs267607738
ensembl	rs267607738
geneview	rs267607738
scholar	rs267607738
google	rs267607738
pharmgkb	rs267607738
gwascentral	rs267607738
openSNP	rs267607738
23andMe	rs267607738
SNPshot	rs267607738
SNPdbe	rs267607738
MSV3d	rs267607738
GWAS Ctlg	rs267607738

Max Magnitude

6

ClinVar
Risk	rs267607738(T;T)
Alt	rs267607738(T;T)
Reference	Rs267607738(-;-)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37042546dupT
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075629.2,