rs267607854

Orientation

plus

Stabilized

plus

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

Make rs267607854(A;A)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37047518

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs267607854
dbSNP (classic)	rs267607854
ClinGen	rs267607854
ebi	rs267607854
HLI	rs267607854
Exac	rs267607854
Gnomad	rs267607854
Varsome	rs267607854
LitVar	rs267607854
Map	rs267607854
PheGenI	rs267607854
Biobank	rs267607854
1000 genomes	rs267607854
hgdp	rs267607854
ensembl	rs267607854
geneview	rs267607854
scholar	rs267607854
google	rs267607854
pharmgkb	rs267607854
gwascentral	rs267607854
openSNP	rs267607854
23andMe	rs267607854
SNPshot	rs267607854
SNPdbe	rs267607854
MSV3d	rs267607854
GWAS Ctlg	rs267607854

Max Magnitude

6

ClinVar
Risk	rs267607854(A;A)
Alt	rs267607854(A;A)
Reference	Rs267607854(G;G)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37089009G>A
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075333.2,