rs267607819

Orientation

minus

Stabilized

minus

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

Make rs267607819(T;T)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37025636

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs267607819
dbSNP (classic)	rs267607819
ClinGen	rs267607819
ebi	rs267607819
HLI	rs267607819
Exac	rs267607819
Gnomad	rs267607819
Varsome	rs267607819
LitVar	rs267607819
Map	rs267607819
PheGenI	rs267607819
Biobank	rs267607819
1000 genomes	rs267607819
hgdp	rs267607819
ensembl	rs267607819
geneview	rs267607819
scholar	rs267607819
google	rs267607819
pharmgkb	rs267607819
gwascentral	rs267607819
openSNP	rs267607819
23andMe	rs267607819
SNPshot	rs267607819
SNPdbe	rs267607819
MSV3d	rs267607819
GWAS Ctlg	rs267607819

Max Magnitude

6

ClinVar
Risk	rs267607819(G;G) rs267607819(T;T)
Alt	rs267607819(G;G) rs267607819(T;T)
Reference	Rs267607819(C;C)
Significance	Pathogenic
Disease	Lynch syndrome not provided
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome not provided
Reversed	1
HGVS	NC_000003.11:g.37067127G>A
CLNSRC	HGMD
CLNACC	RCV000075088.2, RCV000153506.5,