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rs587782285

From SNPedia

Orientationplus
Geno Mag Summary
(GAA;GAA) 0 common in clinvar
Make rs587782285(-;-)
Make rs587782285(-;GAA)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position37047632
GeneMLH1
is asnp
is mentioned by
dbSNPrs587782285
ebirs587782285
HLIrs587782285
Exacrs587782285
Varsomers587782285
Maprs587782285
PheGenIrs587782285
hapmaprs587782285
1000 genomesrs587782285
hgdprs587782285
ensemblrs587782285
gopubmedrs587782285
geneviewrs587782285
scholarrs587782285
googlers587782285
pharmgkbrs587782285
gwascentralrs587782285
openSNPrs587782285
23andMers587782285
23andMe allrs587782285
SNP Nexus

SNPshotrs587782285
SNPdbers587782285
MSV3drs587782285
GWAS Ctlgrs587782285
Max Magnitude0
ClinVar
Risk rs587782285(;)
Alt rs587782285(;)
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 International Society for Gastrointestinal Hereditary Tumours OMIM Allelic Variant
CLNACC RCV000018609.27, RCV000075383.4, RCV000129328.4, RCV000192399.2, RCV000202279.2,