rs63750081

Orientation

plus

Stabilized

plus

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

Make rs63750081(-;-)

Reference

GRCh38 38.1/141

Chromosome

3

Position

36993584

Gene	EPM2AIP1, MLH1

is a	snp
is	mentioned by
dbSNP	rs63750081
dbSNP (classic)	rs63750081
ClinGen	rs63750081
ebi	rs63750081
HLI	rs63750081
Exac	rs63750081
Gnomad	rs63750081
Varsome	rs63750081
LitVar	rs63750081
Map	rs63750081
PheGenI	rs63750081
Biobank	rs63750081
1000 genomes	rs63750081
hgdp	rs63750081
ensembl	rs63750081
geneview	rs63750081
scholar	rs63750081
google	rs63750081
pharmgkb	rs63750081
gwascentral	rs63750081
openSNP	rs63750081
23andMe	rs63750081
SNPshot	rs63750081
SNPdbe	rs63750081
MSV3d	rs63750081
GWAS Ctlg	rs63750081

Max Magnitude

6

ClinVar
Risk	rs63750081(-;-)
Alt	rs63750081(-;-)
Reference	Rs63750081(G;G)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	EPM2AIP1 MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37035075delG
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075678.2,