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rs869312767

From SNPedia

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Geno Mag Summary
(CG;CG) 0 common in clinvar
Make rs869312767(CG;TA)
Make rs869312767(TA;TA)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position36993572
GeneEPM2AIP1, MLH1
is asnp
is mentioned by
dbSNPrs869312767
ebirs869312767
HLIrs869312767
Exacrs869312767
Varsomers869312767
Maprs869312767
PheGenIrs869312767
hapmaprs869312767
1000 genomesrs869312767
hgdprs869312767
ensemblrs869312767
gopubmedrs869312767
geneviewrs869312767
scholarrs869312767
googlers869312767
pharmgkbrs869312767
gwascentralrs869312767
openSNPrs869312767
23andMers869312767
23andMe allrs869312767
SNP Nexus

SNPshotrs869312767
SNPdbers869312767
MSV3drs869312767
GWAS Ctlgrs869312767
Max Magnitude0
ClinVar
Risk rs869312767(TA;TA)
Alt rs869312767(TA;TA)
Reference rs869312767(CG;CG)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene EPM2AIP1 MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37035063_37035064delCGinsTA
CLNSRC
CLNACC RCV000210198.1,