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rs878853794

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs878853794(-;-)
Make rs878853794(-;AG)
Make rs878853794(AG;AG)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position37020387
GeneMLH1
is asnp
is mentioned by
dbSNPrs878853794
ebirs878853794
HLIrs878853794
Exacrs878853794
Varsomers878853794
Maprs878853794
PheGenIrs878853794
hapmaprs878853794
1000 genomesrs878853794
hgdprs878853794
ensemblrs878853794
gopubmedrs878853794
geneviewrs878853794
scholarrs878853794
googlers878853794
pharmgkbrs878853794
gwascentralrs878853794
openSNPrs878853794
23andMers878853794
23andMe allrs878853794
SNP Nexus

SNPshotrs878853794
SNPdbers878853794
MSV3drs878853794
GWAS Ctlgrs878853794
Max Magnitude0
ClinVar
Risk rs878853794(GA;GA)
Alt rs878853794(GA;GA)
Reference rs878853794(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37061877_37061878dupAG
CLNSRC
CLNACC RCV000228583.1,