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rs587778882

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587778882(-;-)
Make rs587778882(-;AA)
Make rs587778882(AA;AA)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position36993651
GeneEPM2AIP1, MLH1
is asnp
is mentioned by
dbSNPrs587778882
ebirs587778882
HLIrs587778882
Exacrs587778882
Varsomers587778882
Maprs587778882
PheGenIrs587778882
hapmaprs587778882
1000 genomesrs587778882
hgdprs587778882
ensemblrs587778882
gopubmedrs587778882
geneviewrs587778882
scholarrs587778882
googlers587778882
pharmgkbrs587778882
gwascentralrs587778882
openSNPrs587778882
23andMers587778882
23andMe allrs587778882
SNP Nexus

SNPshotrs587778882
SNPdbers587778882
MSV3drs587778882
GWAS Ctlgrs587778882
Max Magnitude0
ClinVar
Risk rs587778882(AA;AA)
Alt rs587778882(AA;AA)
Reference rs587778882(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene EPM2AIP1 MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37035142_37035143insAA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075102.2,