rs587778925

Orientation

plus

Stabilized

plus

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

Make rs587778925(-;-)

Reference

GRCh38.p2 38.2/144

Chromosome

3

Position

37028926

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs587778925
dbSNP (classic)	rs587778925
ClinGen	rs587778925
ebi	rs587778925
HLI	rs587778925
Exac	rs587778925
Gnomad	rs587778925
Varsome	rs587778925
LitVar	rs587778925
Map	rs587778925
PheGenI	rs587778925
Biobank	rs587778925
1000 genomes	rs587778925
hgdp	rs587778925
ensembl	rs587778925
geneview	rs587778925
scholar	rs587778925
google	rs587778925
pharmgkb	rs587778925
gwascentral	rs587778925
openSNP	rs587778925
23andMe	rs587778925
SNPshot	rs587778925
SNPdbe	rs587778925
MSV3d	rs587778925
GWAS Ctlg	rs587778925

Max Magnitude

6

ClinVar
Risk	rs587778925(-;-)
Alt	rs587778925(-;-)
Reference	Rs587778925(C;C)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37070417delC
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075241.2,