rs63749827

Orientation

plus

Stabilized

plus

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

Make rs63749827(T;T)

Reference

GRCh38 38.1/141

Chromosome

3

Position

36993623

Gene	EPM2AIP1, MLH1

is a	snp
is	mentioned by
dbSNP	rs63749827
dbSNP (classic)	rs63749827
ClinGen	rs63749827
ebi	rs63749827
HLI	rs63749827
Exac	rs63749827
Gnomad	rs63749827
Varsome	rs63749827
LitVar	rs63749827
Map	rs63749827
PheGenI	rs63749827
Biobank	rs63749827
1000 genomes	rs63749827
hgdp	rs63749827
ensembl	rs63749827
geneview	rs63749827
scholar	rs63749827
google	rs63749827
pharmgkb	rs63749827
gwascentral	rs63749827
openSNP	rs63749827
23andMe	rs63749827
SNPshot	rs63749827
SNPdbe	rs63749827
MSV3d	rs63749827
GWAS Ctlg	rs63749827

Max Magnitude

6

ClinVar
Risk	rs63749827(T;T)
Alt	rs63749827(T;T)
Reference	Rs63749827(C;C)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	EPM2AIP1 MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37035114C>T
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075838.2,