rs267607806

Orientation

plus

Stabilized

plus

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

Make rs267607806(C;C)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37017601

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs267607806
dbSNP (classic)	rs267607806
ClinGen	rs267607806
ebi	rs267607806
HLI	rs267607806
Exac	rs267607806
Gnomad	rs267607806
Varsome	rs267607806
LitVar	rs267607806
Map	rs267607806
PheGenI	rs267607806
Biobank	rs267607806
1000 genomes	rs267607806
hgdp	rs267607806
ensembl	rs267607806
geneview	rs267607806
scholar	rs267607806
google	rs267607806
pharmgkb	rs267607806
gwascentral	rs267607806
openSNP	rs267607806
23andMe	rs267607806
SNPshot	rs267607806
SNPdbe	rs267607806
MSV3d	rs267607806
GWAS Ctlg	rs267607806

Max Magnitude

6

ClinVar
Risk	rs267607806(C;C)
Alt	rs267607806(C;C)
Reference	Rs267607806(T;T)
Significance	Probable-Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37059092T>C
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075904.2,