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rs878853792

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs878853792(-;-)
Make rs878853792(-;A)
Make rs878853792(A;A)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position37017541
GeneMLH1
is asnp
is mentioned by
dbSNPrs878853792
ebirs878853792
HLIrs878853792
Exacrs878853792
Varsomers878853792
Maprs878853792
PheGenIrs878853792
hapmaprs878853792
1000 genomesrs878853792
hgdprs878853792
ensemblrs878853792
gopubmedrs878853792
geneviewrs878853792
scholarrs878853792
googlers878853792
pharmgkbrs878853792
gwascentralrs878853792
openSNPrs878853792
23andMers878853792
23andMe allrs878853792
SNP Nexus

SNPshotrs878853792
SNPdbers878853792
MSV3drs878853792
GWAS Ctlgrs878853792
Max Magnitude0
ClinVar
Risk rs878853792(A;A)
Alt rs878853792(A;A)
Reference rs878853792(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37059032dupA
CLNSRC
CLNACC RCV000231231.1,