rs267607702

Orientation

plus

Stabilized

plus

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

Make rs267607702(-;-)

Reference

GRCh38 38.1/141

Chromosome

3

Position

36993566

Gene	EPM2AIP1, MLH1

is a	snp
is	mentioned by
dbSNP	rs267607702
dbSNP (classic)	rs267607702
ClinGen	rs267607702
ebi	rs267607702
HLI	rs267607702
Exac	rs267607702
Gnomad	rs267607702
Varsome	rs267607702
LitVar	rs267607702
Map	rs267607702
PheGenI	rs267607702
Biobank	rs267607702
1000 genomes	rs267607702
hgdp	rs267607702
ensembl	rs267607702
geneview	rs267607702
scholar	rs267607702
google	rs267607702
pharmgkb	rs267607702
gwascentral	rs267607702
openSNP	rs267607702
23andMe	rs267607702
SNPshot	rs267607702
SNPdbe	rs267607702
MSV3d	rs267607702
GWAS Ctlg	rs267607702

Max Magnitude

6

ClinVar
Risk	rs267607702(-;-)
Alt	rs267607702(-;-)
Reference	Rs267607702(GTTATTCGGCGGCTGGA;GTTATTCGGCGGCTGGA)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	EPM2AIP1 MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37035057_37035073del17
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075476.2,