rs63750581

Orientation

plus

Stabilized

plus

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

Make rs63750581(-;-)

Reference

GRCh38 38.1/141

Chromosome

3

Position

36993608

Gene	EPM2AIP1, MLH1

is a	snp
is	mentioned by
dbSNP	rs63750581
dbSNP (classic)	rs63750581
ClinGen	rs63750581
ebi	rs63750581
HLI	rs63750581
Exac	rs63750581
Gnomad	rs63750581
Varsome	rs63750581
LitVar	rs63750581
Map	rs63750581
PheGenI	rs63750581
Biobank	rs63750581
1000 genomes	rs63750581
hgdp	rs63750581
ensembl	rs63750581
geneview	rs63750581
scholar	rs63750581
google	rs63750581
pharmgkb	rs63750581
gwascentral	rs63750581
openSNP	rs63750581
23andMe	rs63750581
SNPshot	rs63750581
SNPdbe	rs63750581
MSV3d	rs63750581
GWAS Ctlg	rs63750581

Max Magnitude

6

ClinVar
Risk	rs63750581(-;-)
Alt	rs63750581(-;-)
Reference	Rs63750581(G;G)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	EPM2AIP1 MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37035099delG
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075785.2,