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rs111052004

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs111052004(G;G)
Make rs111052004(G;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position36993549
GeneEPM2AIP1, MLH1
is asnp
is mentioned by
dbSNPrs111052004
ebirs111052004
HLIrs111052004
Exacrs111052004
Varsomers111052004
Maprs111052004
PheGenIrs111052004
hapmaprs111052004
1000 genomesrs111052004
hgdprs111052004
ensemblrs111052004
gopubmedrs111052004
geneviewrs111052004
scholarrs111052004
googlers111052004
pharmgkbrs111052004
gwascentralrs111052004
openSNPrs111052004
23andMers111052004
23andMe allrs111052004
SNP Nexus

SNPshotrs111052004
SNPdbers111052004
MSV3drs111052004
GWAS Ctlgrs111052004
Max Magnitude0
ClinVar
Risk rs111052004(A,C,G;A,C,G)
Alt rs111052004(A,C,G;A,C,G)
Reference rs111052004(T;T)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene EPM2AIP1 MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37035040T>A; NC_000003.11:g.37035040T>C; NC_000003.11:g.37035040T>G
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075620.2, RCV000075621.2, RCV000075622.2,