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rs63750656

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs63750656(G;T)
Make rs63750656(T;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position36993632
GeneEPM2AIP1, MLH1
is asnp
is mentioned by
dbSNPrs63750656
ebirs63750656
HLIrs63750656
Exacrs63750656
Varsomers63750656
Maprs63750656
PheGenIrs63750656
hapmaprs63750656
1000 genomesrs63750656
hgdprs63750656
ensemblrs63750656
gopubmedrs63750656
geneviewrs63750656
scholarrs63750656
googlers63750656
pharmgkbrs63750656
gwascentralrs63750656
openSNPrs63750656
23andMers63750656
23andMe allrs63750656
SNP Nexus

SNPshotrs63750656
SNPdbers63750656
MSV3drs63750656
GWAS Ctlgrs63750656
Max Magnitude0


ClinVar
Risk rs63750656(T;T)
Alt rs63750656(T;T)
Reference rs63750656(G;G)
Significance Pathogenic
Disease Lynch syndrome Hereditary cancer-predisposing syndrome not specified
Variation info
Gene EPM2AIP1 MLH1
CLNDBN Lynch syndrome Hereditary cancer-predisposing syndrome not specified
Reversed 0
HGVS NC_000003.11:g.37035123G>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075890.2, RCV000132377.2, RCV000201970.2,