rs267607795

Orientation

plus

Stabilized

plus

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

Make rs267607795(C;C)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37017505

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs267607795
dbSNP (classic)	rs267607795
ClinGen	rs267607795
ebi	rs267607795
HLI	rs267607795
Exac	rs267607795
Gnomad	rs267607795
Varsome	rs267607795
LitVar	rs267607795
Map	rs267607795
PheGenI	rs267607795
Biobank	rs267607795
1000 genomes	rs267607795
hgdp	rs267607795
ensembl	rs267607795
geneview	rs267607795
scholar	rs267607795
google	rs267607795
pharmgkb	rs267607795
gwascentral	rs267607795
openSNP	rs267607795
23andMe	rs267607795
SNPshot	rs267607795
SNPdbe	rs267607795
MSV3d	rs267607795
GWAS Ctlg	rs267607795

Max Magnitude

6

ClinVar
Risk	rs267607795(A;A) rs267607795(C;C) rs267607795(T;T)
Alt	rs267607795(A;A) rs267607795(C;C) rs267607795(T;T)
Reference	Rs267607795(G;G)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37058996G>A; NC_000003.11:g.37058996G>C; NC_000003.11:g.37058996G>T
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000168716.2, RCV000075860.2, RCV000075861.2,