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rs63749876

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs63749876(-;-)
Make rs63749876(-;A)
ReferenceGRCh38 38.1/141
Chromosome3
Position37028837
GeneMLH1
is asnp
is mentioned by
dbSNPrs63749876
ebirs63749876
HLIrs63749876
Exacrs63749876
Varsomers63749876
Maprs63749876
PheGenIrs63749876
hapmaprs63749876
1000 genomesrs63749876
hgdprs63749876
ensemblrs63749876
gopubmedrs63749876
geneviewrs63749876
scholarrs63749876
googlers63749876
pharmgkbrs63749876
gwascentralrs63749876
openSNPrs63749876
23andMers63749876
23andMe allrs63749876
SNP Nexus

SNPshotrs63749876
SNPdbers63749876
MSV3drs63749876
GWAS Ctlgrs63749876
Max Magnitude0
ClinVar
Risk rs63749876(;)
Alt rs63749876(;)
Reference rs63749876(A;A)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37070328delA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075221.2,