rs267607816

Orientation

plus

Stabilized

plus

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

Make rs267607816(C;C)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37020464

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs267607816
dbSNP (classic)	rs267607816
ClinGen	rs267607816
ebi	rs267607816
HLI	rs267607816
Exac	rs267607816
Gnomad	rs267607816
Varsome	rs267607816
LitVar	rs267607816
Map	rs267607816
PheGenI	rs267607816
Biobank	rs267607816
1000 genomes	rs267607816
hgdp	rs267607816
ensembl	rs267607816
geneview	rs267607816
scholar	rs267607816
google	rs267607816
pharmgkb	rs267607816
gwascentral	rs267607816
openSNP	rs267607816
23andMe	rs267607816
SNPshot	rs267607816
SNPdbe	rs267607816
MSV3d	rs267607816
GWAS Ctlg	rs267607816

Max Magnitude

6

ClinVar
Risk	rs267607816(C;C)
Alt	rs267607816(C;C)
Reference	Rs267607816(G;G)
Significance	Probable-Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37061955G>C
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075082.2,