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rs63750822

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs63750822(-;-)
Make rs63750822(-;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position36993614
GeneEPM2AIP1, MLH1
is asnp
is mentioned by
dbSNPrs63750822
ebirs63750822
HLIrs63750822
Exacrs63750822
Varsomers63750822
Maprs63750822
PheGenIrs63750822
hapmaprs63750822
1000 genomesrs63750822
hgdprs63750822
ensemblrs63750822
gopubmedrs63750822
geneviewrs63750822
scholarrs63750822
googlers63750822
pharmgkbrs63750822
gwascentralrs63750822
openSNPrs63750822
23andMers63750822
23andMe allrs63750822
SNP Nexus

SNPshotrs63750822
SNPdbers63750822
MSV3drs63750822
GWAS Ctlgrs63750822
Max Magnitude0
ClinVar
Risk rs63750822(;)
Alt rs63750822(;)
Reference rs63750822(G;G)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene EPM2AIP1 MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37035105delG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075823.2,