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rs63750081

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs63750081(-;-)
Make rs63750081(-;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position36993584
GeneEPM2AIP1, MLH1
is asnp
is mentioned by
dbSNPrs63750081
ebirs63750081
HLIrs63750081
Exacrs63750081
Varsomers63750081
Maprs63750081
PheGenIrs63750081
hapmaprs63750081
1000 genomesrs63750081
hgdprs63750081
ensemblrs63750081
gopubmedrs63750081
geneviewrs63750081
scholarrs63750081
googlers63750081
pharmgkbrs63750081
gwascentralrs63750081
openSNPrs63750081
23andMers63750081
23andMe allrs63750081
SNP Nexus

SNPshotrs63750081
SNPdbers63750081
MSV3drs63750081
GWAS Ctlgrs63750081
Max Magnitude0
ClinVar
Risk rs63750081(;)
Alt rs63750081(;)
Reference rs63750081(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene EPM2AIP1 MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37035075delG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075678.2,