rs267607849

Orientation

plus

Stabilized

plus

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

Make rs267607849(-;-)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37042290

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs267607849
dbSNP (classic)	rs267607849
ClinGen	rs267607849
ebi	rs267607849
HLI	rs267607849
Exac	rs267607849
Gnomad	rs267607849
Varsome	rs267607849
LitVar	rs267607849
Map	rs267607849
PheGenI	rs267607849
Biobank	rs267607849
1000 genomes	rs267607849
hgdp	rs267607849
ensembl	rs267607849
geneview	rs267607849
scholar	rs267607849
google	rs267607849
pharmgkb	rs267607849
gwascentral	rs267607849
openSNP	rs267607849
23andMe	rs267607849
SNPshot	rs267607849
SNPdbe	rs267607849
MSV3d	rs267607849
GWAS Ctlg	rs267607849

Max Magnitude

6

ClinVar
Risk	rs267607849(-;-)
Alt	rs267607849(-;-)
Reference	Rs267607849(ACTC;ACTC)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37083781_37083784delCTCA
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075315.2,