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rs138705565

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs138705565(A;A)
Make rs138705565(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position36993627
GeneEPM2AIP1, MLH1
is asnp
is mentioned by
dbSNPrs138705565
ebirs138705565
HLIrs138705565
Exacrs138705565
Varsomers138705565
Maprs138705565
PheGenIrs138705565
hapmaprs138705565
1000 genomesrs138705565
hgdprs138705565
ensemblrs138705565
gopubmedrs138705565
geneviewrs138705565
scholarrs138705565
googlers138705565
pharmgkbrs138705565
gwascentralrs138705565
openSNPrs138705565
23andMers138705565
23andMe allrs138705565
SNP Nexus

SNPshotrs138705565
SNPdbers138705565
MSV3drs138705565
GWAS Ctlgrs138705565
Max Magnitude0
ClinVar
Risk rs138705565(A;A) rs138705565(C;C)
Alt rs138705565(A;A) rs138705565(C;C)
Reference Rs138705565(G;G)
Significance Probable-Pathogenic
Disease Lynch syndrome not specified
Variation info
Gene EPM2AIP1 MLH1
CLNDBN Lynch syndrome not specified
Reversed 0
HGVS NC_000003.11:g.37035118G>A; NC_000003.11:g.37035118G>C
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000197307.1, RCV000215376.1, RCV000030232.3,