rs138705565

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs138705565(A;A)

Make rs138705565(A;G)

Reference

GRCh38 38.1/141

Chromosome

3

Position

36993627

Gene	EPM2AIP1, MLH1

is a	snp
is	mentioned by
dbSNP	rs138705565
dbSNP (classic)	rs138705565
ClinGen	rs138705565
ebi	rs138705565
HLI	rs138705565
Exac	rs138705565
Gnomad	rs138705565
Varsome	rs138705565
LitVar	rs138705565
Map	rs138705565
PheGenI	rs138705565
Biobank	rs138705565
1000 genomes	rs138705565
hgdp	rs138705565
ensembl	rs138705565
geneview	rs138705565
scholar	rs138705565
google	rs138705565
pharmgkb	rs138705565
gwascentral	rs138705565
openSNP	rs138705565
23andMe	rs138705565
SNPshot	rs138705565
SNPdbe	rs138705565
MSV3d	rs138705565
GWAS Ctlg	rs138705565

Max Magnitude

0

ClinVar
Risk	rs138705565(A;A) rs138705565(C;C)
Alt	rs138705565(A;A) rs138705565(C;C)
Reference	Rs138705565(G;G)
Significance	Probable-Pathogenic
Disease	Lynch syndrome not specified
Variation	info
Gene	EPM2AIP1 MLH1
CLNDBN	Lynch syndrome not specified
Reversed	0
HGVS	NC_000003.11:g.37035118G>A; NC_000003.11:g.37035118G>C
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000197307.2, RCV000215376.1, RCV000030232.3,