rs63751486

Orientation

plus

Stabilized

plus

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

Make rs63751486(-;-)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37047551

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs63751486
dbSNP (classic)	rs63751486
ClinGen	rs63751486
ebi	rs63751486
HLI	rs63751486
Exac	rs63751486
Gnomad	rs63751486
Varsome	rs63751486
LitVar	rs63751486
Map	rs63751486
PheGenI	rs63751486
Biobank	rs63751486
1000 genomes	rs63751486
hgdp	rs63751486
ensembl	rs63751486
geneview	rs63751486
scholar	rs63751486
google	rs63751486
pharmgkb	rs63751486
gwascentral	rs63751486
openSNP	rs63751486
23andMe	rs63751486
SNPshot	rs63751486
SNPdbe	rs63751486
MSV3d	rs63751486
GWAS Ctlg	rs63751486

Max Magnitude

6

ClinVar
Risk	rs63751486(-;-)
Alt	rs63751486(-;-)
Reference	Rs63751486(T;T)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37089042delT
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075359.2,