rs63750855

Orientation

plus

Stabilized

plus

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

Make rs63750855(-;-)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37028863

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs63750855
dbSNP (classic)	rs63750855
ClinGen	rs63750855
ebi	rs63750855
HLI	rs63750855
Exac	rs63750855
Gnomad	rs63750855
Varsome	rs63750855
LitVar	rs63750855
Map	rs63750855
PheGenI	rs63750855
Biobank	rs63750855
1000 genomes	rs63750855
hgdp	rs63750855
ensembl	rs63750855
geneview	rs63750855
scholar	rs63750855
google	rs63750855
pharmgkb	rs63750855
gwascentral	rs63750855
openSNP	rs63750855
23andMe	rs63750855
SNPshot	rs63750855
SNPdbe	rs63750855
MSV3d	rs63750855
GWAS Ctlg	rs63750855

Max Magnitude

6

ClinVar
Risk	rs63750855(-;-)
Alt	rs63750855(-;-)
Reference	Rs63750855(C;C)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37070354delC
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075226.2,