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rs587778888

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587778888(A;G)
Make rs587778888(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position36993660
GeneEPM2AIP1, MLH1
is asnp
is mentioned by
dbSNPrs587778888
ebirs587778888
HLIrs587778888
Exacrs587778888
Varsomers587778888
Maprs587778888
PheGenIrs587778888
hapmaprs587778888
1000 genomesrs587778888
hgdprs587778888
ensemblrs587778888
gopubmedrs587778888
geneviewrs587778888
scholarrs587778888
googlers587778888
pharmgkbrs587778888
gwascentralrs587778888
openSNPrs587778888
23andMers587778888
23andMe allrs587778888
SNP Nexus

SNPshotrs587778888
SNPdbers587778888
MSV3drs587778888
GWAS Ctlgrs587778888
Max Magnitude0
ClinVar
Risk rs587778888(G;G)
Alt rs587778888(G;G)
Reference rs587778888(A;A)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene EPM2AIP1 MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37035151A>G
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075118.2,