rs267607799

Orientation

plus

Stabilized

plus

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

Make rs267607799(-;-)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37017506

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs267607799
dbSNP (classic)	rs267607799
ClinGen	rs267607799
ebi	rs267607799
HLI	rs267607799
Exac	rs267607799
Gnomad	rs267607799
Varsome	rs267607799
LitVar	rs267607799
Map	rs267607799
PheGenI	rs267607799
Biobank	rs267607799
1000 genomes	rs267607799
hgdp	rs267607799
ensembl	rs267607799
geneview	rs267607799
scholar	rs267607799
google	rs267607799
pharmgkb	rs267607799
gwascentral	rs267607799
openSNP	rs267607799
23andMe	rs267607799
SNPshot	rs267607799
SNPdbe	rs267607799
MSV3d	rs267607799
GWAS Ctlg	rs267607799

Max Magnitude

6

ClinVar
Risk	rs267607799(-;-)
Alt	rs267607799(-;-)
Reference	Rs267607799(GATC;GATC)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37058997_37059000delATCG
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075870.2,