rs267607753

Orientation

plus

Stabilized

plus

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

Make rs267607753(G;G)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37008812

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs267607753
dbSNP (classic)	rs267607753
ClinGen	rs267607753
ebi	rs267607753
HLI	rs267607753
Exac	rs267607753
Gnomad	rs267607753
Varsome	rs267607753
LitVar	rs267607753
Map	rs267607753
PheGenI	rs267607753
Biobank	rs267607753
1000 genomes	rs267607753
hgdp	rs267607753
ensembl	rs267607753
geneview	rs267607753
scholar	rs267607753
google	rs267607753
pharmgkb	rs267607753
gwascentral	rs267607753
openSNP	rs267607753
23andMe	rs267607753
SNPshot	rs267607753
SNPdbe	rs267607753
MSV3d	rs267607753
GWAS Ctlg	rs267607753

Max Magnitude

6

ClinVar
Risk	rs267607753(G;G)
Alt	rs267607753(G;G)
Reference	Rs267607753(A;A)
Significance	Probable-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.37050303A>G
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075721.2, RCV000218165.1,