rs63750749

Orientation

plus

Stabilized

plus

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

Make rs63750749(-;-)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37025788

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs63750749
dbSNP (classic)	rs63750749
ClinGen	rs63750749
ebi	rs63750749
HLI	rs63750749
Exac	rs63750749
Gnomad	rs63750749
Varsome	rs63750749
LitVar	rs63750749
Map	rs63750749
PheGenI	rs63750749
Biobank	rs63750749
1000 genomes	rs63750749
hgdp	rs63750749
ensembl	rs63750749
geneview	rs63750749
scholar	rs63750749
google	rs63750749
pharmgkb	rs63750749
gwascentral	rs63750749
openSNP	rs63750749
23andMe	rs63750749
SNPshot	rs63750749
SNPdbe	rs63750749
MSV3d	rs63750749
GWAS Ctlg	rs63750749

Max Magnitude

6

ClinVar
Risk	rs63750749(-;-)
Alt	rs63750749(-;-)
Reference	Rs63750749(T;T)
Significance	Pathogenic
Disease	Lynch syndrome Hereditary cancer-predisposing syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000003.11:g.37067279delT
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075145.2, RCV000165649.1,