rs63750533

Orientation

plus

Stabilized

plus

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

Make rs63750533(-;-)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37020419

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs63750533
dbSNP (classic)	rs63750533
ClinGen	rs63750533
ebi	rs63750533
HLI	rs63750533
Exac	rs63750533
Gnomad	rs63750533
Varsome	rs63750533
LitVar	rs63750533
Map	rs63750533
PheGenI	rs63750533
Biobank	rs63750533
1000 genomes	rs63750533
hgdp	rs63750533
ensembl	rs63750533
geneview	rs63750533
scholar	rs63750533
google	rs63750533
pharmgkb	rs63750533
gwascentral	rs63750533
openSNP	rs63750533
23andMe	rs63750533
SNPshot	rs63750533
SNPdbe	rs63750533
MSV3d	rs63750533
GWAS Ctlg	rs63750533

Max Magnitude

6

ClinVar
Risk	rs63750533(-;-)
Alt	rs63750533(-;-)
Reference	Rs63750533(A;A)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37061910delA
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075956.2,