rs267607794

Orientation

plus

Stabilized

plus

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

Make rs267607794(G;G)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37017504

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs267607794
dbSNP (classic)	rs267607794
ClinGen	rs267607794
ebi	rs267607794
HLI	rs267607794
Exac	rs267607794
Gnomad	rs267607794
Varsome	rs267607794
LitVar	rs267607794
Map	rs267607794
PheGenI	rs267607794
Biobank	rs267607794
1000 genomes	rs267607794
hgdp	rs267607794
ensembl	rs267607794
geneview	rs267607794
scholar	rs267607794
google	rs267607794
pharmgkb	rs267607794
gwascentral	rs267607794
openSNP	rs267607794
23andMe	rs267607794
SNPshot	rs267607794
SNPdbe	rs267607794
MSV3d	rs267607794
GWAS Ctlg	rs267607794

Max Magnitude

6

ClinVar
Risk	rs267607794(G;G) rs267607794(T;T)
Alt	rs267607794(G;G) rs267607794(T;T)
Reference	Rs267607794(A;A)
Significance	Pathogenic
Disease	Lynch syndrome Hereditary cancer-predisposing syndrome not provided
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome Hereditary cancer-predisposing syndrome not provided
Reversed	0
HGVS	NC_000003.11:g.37058995A>G; NC_000003.11:g.37058995A>T
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075863.2, RCV000115486.4, RCV000212525.2, RCV000483260.1,