rs63750764

Orientation

plus

Stabilized

plus

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

Make rs63750764(-;-)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37014447

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs63750764
dbSNP (classic)	rs63750764
ClinGen	rs63750764
ebi	rs63750764
HLI	rs63750764
Exac	rs63750764
Gnomad	rs63750764
Varsome	rs63750764
LitVar	rs63750764
Map	rs63750764
PheGenI	rs63750764
Biobank	rs63750764
1000 genomes	rs63750764
hgdp	rs63750764
ensembl	rs63750764
geneview	rs63750764
scholar	rs63750764
google	rs63750764
pharmgkb	rs63750764
gwascentral	rs63750764
openSNP	rs63750764
23andMe	rs63750764
SNPshot	rs63750764
SNPdbe	rs63750764
MSV3d	rs63750764
GWAS Ctlg	rs63750764

Max Magnitude

6

ClinVar
Risk	rs63750764(-;-)
Alt	rs63750764(-;-)
Reference	Rs63750764(T;T)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37055938delT
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075825.2,