rs587779055

Orientation

plus

Stabilized

plus

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

Make rs587779055(-;-)

Reference

GRCh38.p2 38.2/144

Chromosome

3

Position

37020353

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs587779055
dbSNP (classic)	rs587779055
ClinGen	rs587779055
ebi	rs587779055
HLI	rs587779055
Exac	rs587779055
Gnomad	rs587779055
Varsome	rs587779055
LitVar	rs587779055
Map	rs587779055
PheGenI	rs587779055
Biobank	rs587779055
1000 genomes	rs587779055
hgdp	rs587779055
ensembl	rs587779055
geneview	rs587779055
scholar	rs587779055
google	rs587779055
pharmgkb	rs587779055
gwascentral	rs587779055
openSNP	rs587779055
23andMe	rs587779055
SNPshot	rs587779055
SNPdbe	rs587779055
MSV3d	rs587779055
GWAS Ctlg	rs587779055

Max Magnitude

6

ClinVar
Risk	rs587779055(-;-)
Alt	rs587779055(-;-)
Reference	Rs587779055(A;A)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37061844delA
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075939.2,