Have questions? Visit https://www.reddit.com/r/SNPedia

rs878853787

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs878853787(-;-)
Make rs878853787(-;A)
Make rs878853787(A;A)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position37050631
GeneMLH1
is asnp
is mentioned by
dbSNPrs878853787
ebirs878853787
HLIrs878853787
Exacrs878853787
Varsomers878853787
Maprs878853787
PheGenIrs878853787
hapmaprs878853787
1000 genomesrs878853787
hgdprs878853787
ensemblrs878853787
gopubmedrs878853787
geneviewrs878853787
scholarrs878853787
googlers878853787
pharmgkbrs878853787
gwascentralrs878853787
openSNPrs878853787
23andMers878853787
23andMe allrs878853787
SNP Nexus

SNPshotrs878853787
SNPdbers878853787
MSV3drs878853787
GWAS Ctlgrs878853787
Max Magnitude0
ClinVar
Risk rs878853787(A;A)
Alt rs878853787(A;A)
Reference rs878853787(;)
Significance Probable-Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37092122dupA
CLNSRC
CLNACC RCV000226996.1,