rs587778907

Orientation

plus

Stabilized

plus

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

Make rs587778907(-;-)

Reference

GRCh38.p2 38.2/144

Chromosome

3

Position

37025960

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs587778907
dbSNP (classic)	rs587778907
ClinGen	rs587778907
ebi	rs587778907
HLI	rs587778907
Exac	rs587778907
Gnomad	rs587778907
Varsome	rs587778907
LitVar	rs587778907
Map	rs587778907
PheGenI	rs587778907
Biobank	rs587778907
1000 genomes	rs587778907
hgdp	rs587778907
ensembl	rs587778907
geneview	rs587778907
scholar	rs587778907
google	rs587778907
pharmgkb	rs587778907
gwascentral	rs587778907
openSNP	rs587778907
23andMe	rs587778907
SNPshot	rs587778907
SNPdbe	rs587778907
MSV3d	rs587778907
GWAS Ctlg	rs587778907

Max Magnitude

6

ClinVar
Risk	rs587778907(-;-)
Alt	rs587778907(-;-)
Reference	Rs587778907(G;G)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37067451delG
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075180.2,