rs267607879

Orientation

plus

Stabilized

plus

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

Make rs267607879(A;A)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37048610

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs267607879
dbSNP (classic)	rs267607879
ClinGen	rs267607879
ebi	rs267607879
HLI	rs267607879
Exac	rs267607879
Gnomad	rs267607879
Varsome	rs267607879
LitVar	rs267607879
Map	rs267607879
PheGenI	rs267607879
Biobank	rs267607879
1000 genomes	rs267607879
hgdp	rs267607879
ensembl	rs267607879
geneview	rs267607879
scholar	rs267607879
google	rs267607879
pharmgkb	rs267607879
gwascentral	rs267607879
openSNP	rs267607879
23andMe	rs267607879
SNPshot	rs267607879
SNPdbe	rs267607879
MSV3d	rs267607879
GWAS Ctlg	rs267607879

Max Magnitude

6

ClinVar
Risk	rs267607879(A;A) rs267607879(C;C) rs267607879(T;T)
Alt	rs267607879(A;A) rs267607879(C;C) rs267607879(T;T)
Reference	Rs267607879(G;G)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37090101G>A; NC_000003.11:g.37090101G>C; NC_000003.11:g.37090101G>T
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075455.2, RCV000075456.2, RCV000075457.2,