rs587778883

Orientation

plus

Stabilized

plus

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

Make rs587778883(-;-)

Reference

GRCh38.p2 38.2/144

Chromosome

3

Position

37025648

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs587778883
dbSNP (classic)	rs587778883
ClinGen	rs587778883
ebi	rs587778883
HLI	rs587778883
Exac	rs587778883
Gnomad	rs587778883
Varsome	rs587778883
LitVar	rs587778883
Map	rs587778883
PheGenI	rs587778883
Biobank	rs587778883
1000 genomes	rs587778883
hgdp	rs587778883
ensembl	rs587778883
geneview	rs587778883
scholar	rs587778883
google	rs587778883
pharmgkb	rs587778883
gwascentral	rs587778883
openSNP	rs587778883
23andMe	rs587778883
SNPshot	rs587778883
SNPdbe	rs587778883
MSV3d	rs587778883
GWAS Ctlg	rs587778883

Max Magnitude

6

ClinVar
Risk	rs587778883(-;-)
Alt	rs587778883(-;-)
Reference	Rs587778883(A;A)
Significance	Pathogenic
Disease	Lynch syndrome not provided
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome not provided
Reversed	0
HGVS	NC_000003.11:g.37067139delA
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075103.2, RCV000115450.4,