rs587779031

Orientation

plus

Stabilized

plus

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

Make rs587779031(-;-)

Reference

GRCh38.p2 38.2/144

Chromosome

3

Position

37012094

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs587779031
dbSNP (classic)	rs587779031
ClinGen	rs587779031
ebi	rs587779031
HLI	rs587779031
Exac	rs587779031
Gnomad	rs587779031
Varsome	rs587779031
LitVar	rs587779031
Map	rs587779031
PheGenI	rs587779031
Biobank	rs587779031
1000 genomes	rs587779031
hgdp	rs587779031
ensembl	rs587779031
geneview	rs587779031
scholar	rs587779031
google	rs587779031
pharmgkb	rs587779031
gwascentral	rs587779031
openSNP	rs587779031
23andMe	rs587779031
SNPshot	rs587779031
SNPdbe	rs587779031
MSV3d	rs587779031
GWAS Ctlg	rs587779031

Max Magnitude

6

ClinVar
Risk	rs587779031(-;-)
Alt	rs587779031(-;-)
Reference	Rs587779031(T;T)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37053585delT
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075799.2,