rs587778950

Orientation

plus

Stabilized

plus

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

Make rs587778950(-;-)

Reference

GRCh38.p2 38.2/144

Chromosome

3

Position

37047653

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs587778950
dbSNP (classic)	rs587778950
ClinGen	rs587778950
ebi	rs587778950
HLI	rs587778950
Exac	rs587778950
Gnomad	rs587778950
Varsome	rs587778950
LitVar	rs587778950
Map	rs587778950
PheGenI	rs587778950
Biobank	rs587778950
1000 genomes	rs587778950
hgdp	rs587778950
ensembl	rs587778950
geneview	rs587778950
scholar	rs587778950
google	rs587778950
pharmgkb	rs587778950
gwascentral	rs587778950
openSNP	rs587778950
23andMe	rs587778950
SNPshot	rs587778950
SNPdbe	rs587778950
MSV3d	rs587778950
GWAS Ctlg	rs587778950

Max Magnitude

6

ClinVar
Risk	rs587778950(-;-)
Alt	rs587778950(-;-)
Reference	Rs587778950(T;T)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37089144delT
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075391.2,