rs267607715

Orientation

plus

Stabilized

plus

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

Make rs267607715(-;-)

Reference

GRCh38 38.1/141

Chromosome

3

Position

36996697

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs267607715
dbSNP (classic)	rs267607715
ClinGen	rs267607715
ebi	rs267607715
HLI	rs267607715
Exac	rs267607715
Gnomad	rs267607715
Varsome	rs267607715
LitVar	rs267607715
Map	rs267607715
PheGenI	rs267607715
Biobank	rs267607715
1000 genomes	rs267607715
hgdp	rs267607715
ensembl	rs267607715
geneview	rs267607715
scholar	rs267607715
google	rs267607715
pharmgkb	rs267607715
gwascentral	rs267607715
openSNP	rs267607715
23andMe	rs267607715
SNPshot	rs267607715
SNPdbe	rs267607715
MSV3d	rs267607715
GWAS Ctlg	rs267607715

Max Magnitude

6

ClinVar
Risk	rs267607715(-;-)
Alt	rs267607715(-;-)
Reference	Rs267607715(C;C)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37038188delC
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075438.2,