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rs63750706

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63750706(C;T)
Make rs63750706(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position36993609
GeneEPM2AIP1, MLH1
is asnp
is mentioned by
dbSNPrs63750706
ebirs63750706
HLIrs63750706
Exacrs63750706
Varsomers63750706
Maprs63750706
PheGenIrs63750706
hapmaprs63750706
1000 genomesrs63750706
hgdprs63750706
ensemblrs63750706
gopubmedrs63750706
geneviewrs63750706
scholarrs63750706
googlers63750706
pharmgkbrs63750706
gwascentralrs63750706
openSNPrs63750706
23andMers63750706
23andMe allrs63750706
SNP Nexus

SNPshotrs63750706
SNPdbers63750706
MSV3drs63750706
GWAS Ctlgrs63750706
Max Magnitude0
ClinVar
Risk rs63750706(A,T;A,T)
Alt rs63750706(A,T;A,T)
Reference rs63750706(C;C)
Significance Pathogenic
Disease Lynch syndrome Lynch syndrome I
Variation info
Gene EPM2AIP1 MLH1
CLNDBN Lynch syndrome Lynch syndrome I
Reversed 0
HGVS NC_000003.11:g.37035100C>A; NC_000003.11:g.37035100C>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075786.2, RCV000075787.3,