rs63750859

Orientation

plus

Stabilized

plus

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

Make rs63750859(-;-)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37049006

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs63750859
dbSNP (classic)	rs63750859
ClinGen	rs63750859
ebi	rs63750859
HLI	rs63750859
Exac	rs63750859
Gnomad	rs63750859
Varsome	rs63750859
LitVar	rs63750859
Map	rs63750859
PheGenI	rs63750859
Biobank	rs63750859
1000 genomes	rs63750859
hgdp	rs63750859
ensembl	rs63750859
geneview	rs63750859
scholar	rs63750859
google	rs63750859
pharmgkb	rs63750859
gwascentral	rs63750859
openSNP	rs63750859
23andMe	rs63750859
SNPshot	rs63750859
SNPdbe	rs63750859
MSV3d	rs63750859
GWAS Ctlg	rs63750859

Max Magnitude

6

ClinVar
Risk	rs63750859(-;-)
Alt	rs63750859(-;-)
Reference	Rs63750859(CT;CT)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37090497_37090498delTC
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075524.2,