rs587778928

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;GT)	6	Lynch syndrome, pathogenic mutation
(GT;GT)	0	common/normal
(TG;TG)	0	common in clinvar

Make rs587778928(-;-)

Reference

GRCh38.p2 38.2/144

Chromosome

3

Position

37040199

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs587778928
dbSNP (classic)	rs587778928
ClinGen	rs587778928
ebi	rs587778928
HLI	rs587778928
Exac	rs587778928
Gnomad	rs587778928
Varsome	rs587778928
LitVar	rs587778928
Map	rs587778928
PheGenI	rs587778928
Biobank	rs587778928
1000 genomes	rs587778928
hgdp	rs587778928
ensembl	rs587778928
geneview	rs587778928
scholar	rs587778928
google	rs587778928
pharmgkb	rs587778928
gwascentral	rs587778928
openSNP	rs587778928
23andMe	rs587778928
SNPshot	rs587778928
SNPdbe	rs587778928
MSV3d	rs587778928
GWAS Ctlg	rs587778928

Max Magnitude

6

ClinVar
Risk	rs587778928(-;-)
Alt	rs587778928(-;-)
Reference	Rs587778928(TG;TG)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37081690_37081691delGT
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075269.2,