rs587782285

Merged into

rs63751247

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(GAA;GAA)	0	common in clinvar

Make rs587782285(-;-)

Make rs587782285(-;GAA)

Reference

GRCh38.p2 38.2/144

Chromosome

3

Position

37047632

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs587782285
dbSNP (classic)	rs587782285
ClinGen	rs587782285
ebi	rs587782285
HLI	rs587782285
Exac	rs587782285
Gnomad	rs587782285
Varsome	rs587782285
LitVar	rs587782285
Map	rs587782285
PheGenI	rs587782285
Biobank	rs587782285
1000 genomes	rs587782285
hgdp	rs587782285
ensembl	rs587782285
geneview	rs587782285
scholar	rs587782285
google	rs587782285
pharmgkb	rs587782285
gwascentral	rs587782285
openSNP	rs587782285
23andMe	rs587782285
SNPshot	rs587782285
SNPdbe	rs587782285
MSV3d	rs587782285
GWAS Ctlg	rs587782285

Status

Merged into rs63751247

Max Magnitude

0

ClinVar
Risk
Alt
Reference	Rs587782285(GAA;GAA)
Significance	Pathogenic
Disease	Turcot syndrome Lynch syndrome Hereditary cancer-predisposing syndrome Lynch syndrome II not provided
Variation	info
Gene	MLH1
CLNDBN	Turcot syndrome Lynch syndrome Hereditary cancer-predisposing syndrome Lynch syndrome II not provided
Reversed	0
HGVS	NC_000003.11:g.37089130_37089132delAAG
CLNSRC	Children's Hospital of Eastern Ontario International Society for Gastrointestinal Hereditary Tumours OMIM Allelic Variant
CLNACC	RCV000018609.27, RCV000075383.4, RCV000129328.4, RCV000192399.2, RCV000202279.2,