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rs587779040

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587779040(-;-)
Make rs587779040(-;G)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position36993625
GeneEPM2AIP1, MLH1
is asnp
is mentioned by
dbSNPrs587779040
ebirs587779040
HLIrs587779040
Exacrs587779040
Varsomers587779040
Maprs587779040
PheGenIrs587779040
hapmaprs587779040
1000 genomesrs587779040
hgdprs587779040
ensemblrs587779040
gopubmedrs587779040
geneviewrs587779040
scholarrs587779040
googlers587779040
pharmgkbrs587779040
gwascentralrs587779040
openSNPrs587779040
23andMers587779040
23andMe allrs587779040
SNP Nexus

SNPshotrs587779040
SNPdbers587779040
MSV3drs587779040
GWAS Ctlgrs587779040
Max Magnitude0
ClinVar
Risk rs587779040(;)
Alt rs587779040(;)
Reference rs587779040(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene EPM2AIP1 MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37035116delG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075845.2,