rs63751651

Orientation

plus

Stabilized

plus

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

Make rs63751651(-;-)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37050486

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs63751651
dbSNP (classic)	rs63751651
ClinGen	rs63751651
ebi	rs63751651
HLI	rs63751651
Exac	rs63751651
Gnomad	rs63751651
Varsome	rs63751651
LitVar	rs63751651
Map	rs63751651
PheGenI	rs63751651
Biobank	rs63751651
1000 genomes	rs63751651
hgdp	rs63751651
ensembl	rs63751651
geneview	rs63751651
scholar	rs63751651
google	rs63751651
pharmgkb	rs63751651
gwascentral	rs63751651
openSNP	rs63751651
23andMe	rs63751651
SNPshot	rs63751651
SNPdbe	rs63751651
MSV3d	rs63751651
GWAS Ctlg	rs63751651

Max Magnitude

6

ClinVar
Risk	rs63751651(-;-)
Alt	rs63751651(-;-)
Reference	Rs63751651(AG;AG)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37091977_37091978delAG
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075544.2,