rs267607845

Orientation

plus

Stabilized

plus

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

Make rs267607845(A;A)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37042267

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs267607845
dbSNP (classic)	rs267607845
ClinGen	rs267607845
ebi	rs267607845
HLI	rs267607845
Exac	rs267607845
Gnomad	rs267607845
Varsome	rs267607845
LitVar	rs267607845
Map	rs267607845
PheGenI	rs267607845
Biobank	rs267607845
1000 genomes	rs267607845
hgdp	rs267607845
ensembl	rs267607845
geneview	rs267607845
scholar	rs267607845
google	rs267607845
pharmgkb	rs267607845
gwascentral	rs267607845
openSNP	rs267607845
23andMe	rs267607845
SNPshot	rs267607845
SNPdbe	rs267607845
MSV3d	rs267607845
GWAS Ctlg	rs267607845

Max Magnitude

6

ClinVar
Risk	rs267607845(A;A) rs267607845(T;T)
Alt	rs267607845(A;A) rs267607845(T;T)
Reference	Rs267607845(G;G)
Significance	Pathogenic
Disease	Lynch syndrome Hereditary cancer-predisposing syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000003.11:g.37083758G>A; NC_000003.11:g.37083758G>T
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075300.2, RCV000214110.1, RCV000075301.2,