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rs587779013

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587779013(-;-)
Make rs587779013(-;GA)
Make rs587779013(GA;GA)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position36993587
GeneEPM2AIP1, MLH1
is asnp
is mentioned by
dbSNPrs587779013
ebirs587779013
HLIrs587779013
Exacrs587779013
Varsomers587779013
Maprs587779013
PheGenIrs587779013
hapmaprs587779013
1000 genomesrs587779013
hgdprs587779013
ensemblrs587779013
gopubmedrs587779013
geneviewrs587779013
scholarrs587779013
googlers587779013
pharmgkbrs587779013
gwascentralrs587779013
openSNPrs587779013
23andMers587779013
23andMe allrs587779013
SNP Nexus

SNPshotrs587779013
SNPdbers587779013
MSV3drs587779013
GWAS Ctlgrs587779013
Max Magnitude0
ClinVar
Risk rs587779013(GA;GA)
Alt rs587779013(GA;GA)
Reference rs587779013(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene EPM2AIP1 MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37035077_37035078dupGA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075699.2,