rs267607710

Orientation

plus

Stabilized

plus

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

Make rs267607710(C;C)

Reference

GRCh38 38.1/141

Chromosome

3

Position

36993668

Gene	EPM2AIP1, MLH1

is a	snp
is	mentioned by
dbSNP	rs267607710
dbSNP (classic)	rs267607710
ClinGen	rs267607710
ebi	rs267607710
HLI	rs267607710
Exac	rs267607710
Gnomad	rs267607710
Varsome	rs267607710
LitVar	rs267607710
Map	rs267607710
PheGenI	rs267607710
Biobank	rs267607710
1000 genomes	rs267607710
hgdp	rs267607710
ensembl	rs267607710
geneview	rs267607710
scholar	rs267607710
google	rs267607710
pharmgkb	rs267607710
gwascentral	rs267607710
openSNP	rs267607710
23andMe	rs267607710
SNPshot	rs267607710
SNPdbe	rs267607710
MSV3d	rs267607710
GWAS Ctlg	rs267607710

Max Magnitude

6

ClinVar
Risk	rs267607710(A;A) rs267607710(C;C)
Alt	rs267607710(A;A) rs267607710(C;C)
Reference	Rs267607710(G;G)
Significance	Pathogenic
Disease	not specified Lynch syndrome not provided
Variation	info
Gene	EPM2AIP1 MLH1
CLNDBN	not specified Lynch syndrome not provided
Reversed	0
HGVS	NC_000003.11:g.37035159G>A; NC_000003.11:g.37035159G>C
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000202146.1, RCV000075129.2, RCV000413453.1,