rs267607850

Orientation

plus

Stabilized

plus

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

Make rs267607850(A;A)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37042336

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs267607850
dbSNP (classic)	rs267607850
ClinGen	rs267607850
ebi	rs267607850
HLI	rs267607850
Exac	rs267607850
Gnomad	rs267607850
Varsome	rs267607850
LitVar	rs267607850
Map	rs267607850
PheGenI	rs267607850
Biobank	rs267607850
1000 genomes	rs267607850
hgdp	rs267607850
ensembl	rs267607850
geneview	rs267607850
scholar	rs267607850
google	rs267607850
pharmgkb	rs267607850
gwascentral	rs267607850
openSNP	rs267607850
23andMe	rs267607850
SNPshot	rs267607850
SNPdbe	rs267607850
MSV3d	rs267607850
GWAS Ctlg	rs267607850

Max Magnitude

6

ClinVar
Risk	rs267607850(A;A)
Alt	rs267607850(A;A)
Reference	Rs267607850(G;G)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37083827G>A
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075328.2,