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rs878853780

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs878853780(C;C)
Make rs878853780(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position37040296
GeneMLH1
is asnp
is mentioned by
dbSNPrs878853780
ebirs878853780
HLIrs878853780
Exacrs878853780
Varsomers878853780
Maprs878853780
PheGenIrs878853780
hapmaprs878853780
1000 genomesrs878853780
hgdprs878853780
ensemblrs878853780
gopubmedrs878853780
geneviewrs878853780
scholarrs878853780
googlers878853780
pharmgkbrs878853780
gwascentralrs878853780
openSNPrs878853780
23andMers878853780
23andMe allrs878853780
SNP Nexus

SNPshotrs878853780
SNPdbers878853780
MSV3drs878853780
GWAS Ctlgrs878853780
Max Magnitude0
ClinVar
Risk rs878853780(C;C)
Alt rs878853780(C;C)
Reference rs878853780(T;T)
Significance Probable-Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37081787T>C
CLNSRC
CLNACC RCV000231513.1,