rs63750740

Orientation

plus

Stabilized

plus

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

Make rs63750740(-;-)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37048923

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs63750740
dbSNP (classic)	rs63750740
ClinGen	rs63750740
ebi	rs63750740
HLI	rs63750740
Exac	rs63750740
Gnomad	rs63750740
Varsome	rs63750740
LitVar	rs63750740
Map	rs63750740
PheGenI	rs63750740
Biobank	rs63750740
1000 genomes	rs63750740
hgdp	rs63750740
ensembl	rs63750740
geneview	rs63750740
scholar	rs63750740
google	rs63750740
pharmgkb	rs63750740
gwascentral	rs63750740
openSNP	rs63750740
23andMe	rs63750740
SNPshot	rs63750740
SNPdbe	rs63750740
MSV3d	rs63750740
GWAS Ctlg	rs63750740

Max Magnitude

6

ClinVar
Risk	rs63750740(-;-)
Alt	rs63750740(-;-)
Reference	Rs63750740(A;A)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37090414delA
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075481.2,