rs63750309

Orientation

plus

Stabilized

plus

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

Make rs63750309(-;-)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37047536

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs63750309
dbSNP (classic)	rs63750309
ClinGen	rs63750309
ebi	rs63750309
HLI	rs63750309
Exac	rs63750309
Gnomad	rs63750309
Varsome	rs63750309
LitVar	rs63750309
Map	rs63750309
PheGenI	rs63750309
Biobank	rs63750309
1000 genomes	rs63750309
hgdp	rs63750309
ensembl	rs63750309
geneview	rs63750309
scholar	rs63750309
google	rs63750309
pharmgkb	rs63750309
gwascentral	rs63750309
openSNP	rs63750309
23andMe	rs63750309
SNPshot	rs63750309
SNPdbe	rs63750309
MSV3d	rs63750309
GWAS Ctlg	rs63750309

Max Magnitude

6

ClinVar
Risk	rs63750309(-;-)
Alt	rs63750309(-;-)
Reference	Rs63750309(T;T)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37089027delT
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075350.2,