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rs878853777

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs878853777(-;-)
Make rs878853777(-;A)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position37028815
GeneMLH1
is asnp
is mentioned by
dbSNPrs878853777
ebirs878853777
HLIrs878853777
Exacrs878853777
Varsomers878853777
Maprs878853777
PheGenIrs878853777
hapmaprs878853777
1000 genomesrs878853777
hgdprs878853777
ensemblrs878853777
gopubmedrs878853777
geneviewrs878853777
scholarrs878853777
googlers878853777
pharmgkbrs878853777
gwascentralrs878853777
openSNPrs878853777
23andMers878853777
23andMe allrs878853777
SNP Nexus

SNPshotrs878853777
SNPdbers878853777
MSV3drs878853777
GWAS Ctlgrs878853777
Max Magnitude0
ClinVar
Risk rs878853777(;)
Alt rs878853777(;)
Reference rs878853777(A;A)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37070306delA
CLNSRC
CLNACC RCV000229125.1,