rs267607709

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;G)	6	Lynch syndrome, pathogenic mutation
(G;G)	0	common in clinvar
(G;T)	6	Lynch syndrome

Make rs267607709(A;A)

Reference

GRCh38 38.1/141

Chromosome

3

Position

36993664

Gene	EPM2AIP1, MLH1

is a	snp
is	mentioned by
dbSNP	rs267607709
dbSNP (classic)	rs267607709
ClinGen	rs267607709
ebi	rs267607709
HLI	rs267607709
Exac	rs267607709
Gnomad	rs267607709
Varsome	rs267607709
LitVar	rs267607709
Map	rs267607709
PheGenI	rs267607709
Biobank	rs267607709
1000 genomes	rs267607709
hgdp	rs267607709
ensembl	rs267607709
geneview	rs267607709
scholar	rs267607709
google	rs267607709
pharmgkb	rs267607709
gwascentral	rs267607709
openSNP	rs267607709
23andMe	rs267607709
SNPshot	rs267607709
SNPdbe	rs267607709
MSV3d	rs267607709
GWAS Ctlg	rs267607709

Max Magnitude

6

ClinVar
Risk	rs267607709(A;A)
Alt	rs267607709(A;A)
Reference	Rs267607709(G;G)
Significance	Probable-Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	EPM2AIP1 MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37035155G>A
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075127.2,