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rs63749906

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs63749906(G;G)
Make rs63749906(G;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position36993651
GeneEPM2AIP1, MLH1
is asnp
is mentioned by
dbSNPrs63749906
ebirs63749906
HLIrs63749906
Exacrs63749906
Varsomers63749906
Maprs63749906
PheGenIrs63749906
hapmaprs63749906
1000 genomesrs63749906
hgdprs63749906
ensemblrs63749906
gopubmedrs63749906
geneviewrs63749906
scholarrs63749906
googlers63749906
pharmgkbrs63749906
gwascentralrs63749906
openSNPrs63749906
23andMers63749906
23andMe allrs63749906
SNP Nexus

SNPshotrs63749906
SNPdbers63749906
MSV3drs63749906
GWAS Ctlgrs63749906
Max Magnitude0
ClinVar
Risk rs63749906(G;G)
Alt rs63749906(G;G)
Reference rs63749906(T;T)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene EPM2AIP1 MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37035142T>G
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075100.2,