rs63750645

Orientation

plus

Stabilized

plus

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

Make rs63750645(-;-)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37004435

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs63750645
dbSNP (classic)	rs63750645
ClinGen	rs63750645
ebi	rs63750645
HLI	rs63750645
Exac	rs63750645
Gnomad	rs63750645
Varsome	rs63750645
LitVar	rs63750645
Map	rs63750645
PheGenI	rs63750645
Biobank	rs63750645
1000 genomes	rs63750645
hgdp	rs63750645
ensembl	rs63750645
geneview	rs63750645
scholar	rs63750645
google	rs63750645
pharmgkb	rs63750645
gwascentral	rs63750645
openSNP	rs63750645
23andMe	rs63750645
SNPshot	rs63750645
SNPdbe	rs63750645
MSV3d	rs63750645
GWAS Ctlg	rs63750645

Max Magnitude

6

ClinVar
Risk	rs63750645(-;-)
Alt	rs63750645(-;-)
Reference	Rs63750645(C;C)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37045926delC
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075660.2,