rs267607699

Orientation

plus

Stabilized

plus

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

Make rs267607699(AAGT;AAGT)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37040291

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs267607699
dbSNP (classic)	rs267607699
ClinGen	rs267607699
ebi	rs267607699
HLI	rs267607699
Exac	rs267607699
Gnomad	rs267607699
Varsome	rs267607699
LitVar	rs267607699
Map	rs267607699
PheGenI	rs267607699
Biobank	rs267607699
1000 genomes	rs267607699
hgdp	rs267607699
ensembl	rs267607699
geneview	rs267607699
scholar	rs267607699
google	rs267607699
pharmgkb	rs267607699
gwascentral	rs267607699
openSNP	rs267607699
23andMe	rs267607699
SNPshot	rs267607699
SNPdbe	rs267607699
MSV3d	rs267607699
GWAS Ctlg	rs267607699

Max Magnitude

6

ClinVar
Risk	rs267607699(TAAG;TAAG)
Alt	rs267607699(TAAG;TAAG)
Reference	Rs267607699(-;-)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37081782_37081783insAAGT
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075297.2,