rs786203456

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;G)	6	Lynch syndrome
(G;G)	0	common in clinvar
(I;I)	0	common genotype

Make rs786203456(-;-)

Reference

GRCh38.p2 38.2/146

Chromosome

3

Position

37047645

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs786203456
dbSNP (classic)	rs786203456
ClinGen	rs786203456
ebi	rs786203456
HLI	rs786203456
Exac	rs786203456
Gnomad	rs786203456
Varsome	rs786203456
LitVar	rs786203456
Map	rs786203456
PheGenI	rs786203456
Biobank	rs786203456
1000 genomes	rs786203456
hgdp	rs786203456
ensembl	rs786203456
geneview	rs786203456
scholar	rs786203456
google	rs786203456
pharmgkb	rs786203456
gwascentral	rs786203456
openSNP	rs786203456
23andMe	rs786203456
SNPshot	rs786203456
SNPdbe	rs786203456
MSV3d	rs786203456
GWAS Ctlg	rs786203456

Max Magnitude

6

ClinVar
Risk	rs786203456(-;-)
Alt	rs786203456(-;-)
Reference	Rs786203456(G;G)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	MLH1
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000003.11:g.37089136delG
CLNSRC
CLNACC	RCV000166770.1,