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rs587779001

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587779001(A;A)
Make rs587779001(A;C)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position36993521
GeneEPM2AIP1, MLH1
is asnp
is mentioned by
dbSNPrs587779001
ebirs587779001
HLIrs587779001
Exacrs587779001
Varsomers587779001
Maprs587779001
PheGenIrs587779001
hapmaprs587779001
1000 genomesrs587779001
hgdprs587779001
ensemblrs587779001
gopubmedrs587779001
geneviewrs587779001
scholarrs587779001
googlers587779001
pharmgkbrs587779001
gwascentralrs587779001
openSNPrs587779001
23andMers587779001
23andMe allrs587779001
SNP Nexus

SNPshotrs587779001
SNPdbers587779001
MSV3drs587779001
GWAS Ctlgrs587779001
Max Magnitude0
ClinVar
Risk rs587779001(A,T;A,T)
Alt rs587779001(A,T;A,T)
Reference rs587779001(C;C)
Significance Pathogenic
Disease Lynch syndrome Hereditary cancer-predisposing syndrome not provided
Variation info
Gene EPM2AIP1 MLH1
CLNDBN Lynch syndrome Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000003.11:g.37035012C>A; NC_000003.11:g.37035012C>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075058.2, RCV000132376.1, RCV000214578.1, RCV000205332.1,