rs267607722

Orientation

plus

Stabilized

plus

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

Make rs267607722(C;C)

Reference

GRCh38 38.1/141

Chromosome

3

Position

36996711

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs267607722
dbSNP (classic)	rs267607722
ClinGen	rs267607722
ebi	rs267607722
HLI	rs267607722
Exac	rs267607722
Gnomad	rs267607722
Varsome	rs267607722
LitVar	rs267607722
Map	rs267607722
PheGenI	rs267607722
Biobank	rs267607722
1000 genomes	rs267607722
hgdp	rs267607722
ensembl	rs267607722
geneview	rs267607722
scholar	rs267607722
google	rs267607722
pharmgkb	rs267607722
gwascentral	rs267607722
openSNP	rs267607722
23andMe	rs267607722
SNPshot	rs267607722
SNPdbe	rs267607722
MSV3d	rs267607722
GWAS Ctlg	rs267607722

Max Magnitude

6

ClinVar
Risk	rs267607722(C;C)
Alt	rs267607722(C;C)
Reference	Rs267607722(T;T)
Significance	Probable-Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37038202T>C
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075508.2,