rs267607867

Orientation

plus

Stabilized

plus

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

Make rs267607867(A;A)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37047684

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs267607867
dbSNP (classic)	rs267607867
ClinGen	rs267607867
ebi	rs267607867
HLI	rs267607867
Exac	rs267607867
Gnomad	rs267607867
Varsome	rs267607867
LitVar	rs267607867
Map	rs267607867
PheGenI	rs267607867
Biobank	rs267607867
1000 genomes	rs267607867
hgdp	rs267607867
ensembl	rs267607867
geneview	rs267607867
scholar	rs267607867
google	rs267607867
pharmgkb	rs267607867
gwascentral	rs267607867
openSNP	rs267607867
23andMe	rs267607867
SNPshot	rs267607867
SNPdbe	rs267607867
MSV3d	rs267607867
GWAS Ctlg	rs267607867

Max Magnitude

6

ClinVar
Risk	rs267607867(A;A) rs267607867(T;T)
Alt	rs267607867(A;A) rs267607867(T;T)
Reference	Rs267607867(G;G)
Significance	Probable-Pathogenic
Disease	Lynch syndrome not provided
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome not provided
Reversed	0
HGVS	NC_000003.11:g.37089175G>A; NC_000003.11:g.37089175G>T
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075404.2, RCV000075405.2, RCV000479456.1,