rs267607894

Orientation

plus

Stabilized

plus

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

Make rs267607894(C;C)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37050628

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs267607894
dbSNP (classic)	rs267607894
ClinGen	rs267607894
ebi	rs267607894
HLI	rs267607894
Exac	rs267607894
Gnomad	rs267607894
Varsome	rs267607894
LitVar	rs267607894
Map	rs267607894
PheGenI	rs267607894
Biobank	rs267607894
1000 genomes	rs267607894
hgdp	rs267607894
ensembl	rs267607894
geneview	rs267607894
scholar	rs267607894
google	rs267607894
pharmgkb	rs267607894
gwascentral	rs267607894
openSNP	rs267607894
23andMe	rs267607894
SNPshot	rs267607894
SNPdbe	rs267607894
MSV3d	rs267607894
GWAS Ctlg	rs267607894

Max Magnitude

6

ClinVar
Risk	rs267607894(A;A) rs267607894(C;C)
Alt	rs267607894(A;A) rs267607894(C;C)
Reference	Rs267607894(T;T)
Significance	Pathogenic
Disease	Lynch syndrome Hereditary cancer-predisposing syndrome not provided
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome Hereditary cancer-predisposing syndrome not provided
Reversed	0
HGVS	NC_000003.11:g.37092119T>C
CLNSRC	UniProtKB (protein)
CLNACC	RCV000075583.2, RCV000216146.1, RCV000478074.1,