rs587781892

Orientation

plus

Stabilized

plus

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

Make rs587781892(-;-)

Reference

GRCh38.p2 38.2/144

Chromosome

3

Position

37025999

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs587781892
dbSNP (classic)	rs587781892
ClinGen	rs587781892
ebi	rs587781892
HLI	rs587781892
Exac	rs587781892
Gnomad	rs587781892
Varsome	rs587781892
LitVar	rs587781892
Map	rs587781892
PheGenI	rs587781892
Biobank	rs587781892
1000 genomes	rs587781892
hgdp	rs587781892
ensembl	rs587781892
geneview	rs587781892
scholar	rs587781892
google	rs587781892
pharmgkb	rs587781892
gwascentral	rs587781892
openSNP	rs587781892
23andMe	rs587781892
SNPshot	rs587781892
SNPdbe	rs587781892
MSV3d	rs587781892
GWAS Ctlg	rs587781892

Max Magnitude

6

ClinVar
Risk	rs587781892(-;-)
Alt	rs587781892(-;-)
Reference	Rs587781892(C;C)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	MLH1
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000003.11:g.37067490delC
CLNSRC
CLNACC	RCV000130228.2,