rs587779009

Orientation

plus

Stabilized

plus

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

Make rs587779009(-;-)

Reference

GRCh38.p2 38.2/144

Chromosome

3

Position

37006998

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs587779009
dbSNP (classic)	rs587779009
ClinGen	rs587779009
ebi	rs587779009
HLI	rs587779009
Exac	rs587779009
Gnomad	rs587779009
Varsome	rs587779009
LitVar	rs587779009
Map	rs587779009
PheGenI	rs587779009
Biobank	rs587779009
1000 genomes	rs587779009
hgdp	rs587779009
ensembl	rs587779009
geneview	rs587779009
scholar	rs587779009
google	rs587779009
pharmgkb	rs587779009
gwascentral	rs587779009
openSNP	rs587779009
23andMe	rs587779009
SNPshot	rs587779009
SNPdbe	rs587779009
MSV3d	rs587779009
GWAS Ctlg	rs587779009

Max Magnitude

6

ClinVar
Risk	rs587779009(-;-)
Alt	rs587779009(-;-)
Reference	Rs587779009(T;T)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37048489delT
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075692.2,