rs267607900

Orientation

plus

Stabilized

plus

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

Make rs267607900(A;T)

Make rs267607900(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

3

Position

37050645

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs267607900
dbSNP (classic)	rs267607900
ClinGen	rs267607900
ebi	rs267607900
HLI	rs267607900
Exac	rs267607900
Gnomad	rs267607900
Varsome	rs267607900
LitVar	rs267607900
Map	rs267607900
PheGenI	rs267607900
Biobank	rs267607900
1000 genomes	rs267607900
hgdp	rs267607900
ensembl	rs267607900
geneview	rs267607900
scholar	rs267607900
google	rs267607900
pharmgkb	rs267607900
gwascentral	rs267607900
openSNP	rs267607900
23andMe	rs267607900
SNPshot	rs267607900
SNPdbe	rs267607900
MSV3d	rs267607900
GWAS Ctlg	rs267607900

Max Magnitude

6

ClinVar
Risk	rs267607900(G;G) rs267607900(T;T)
Alt	rs267607900(G;G) rs267607900(T;T)
Reference	Rs267607900(A;A)
Significance	Pathogenic
Disease	Lynch syndrome I Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome I Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37092136A>G; NC_000003.11:g.37092136A>T
CLNSRC	UniProtKB (protein)
CLNACC	RCV000206724.1, RCV000075591.2,