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

rs878853778

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs878853778(-;-)
Make rs878853778(-;T)
Make rs878853778(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position37028830
GeneMLH1
is asnp
is mentioned by
dbSNPrs878853778
ebirs878853778
HLIrs878853778
Exacrs878853778
Varsomers878853778
Maprs878853778
PheGenIrs878853778
hapmaprs878853778
1000 genomesrs878853778
hgdprs878853778
ensemblrs878853778
gopubmedrs878853778
geneviewrs878853778
scholarrs878853778
googlers878853778
pharmgkbrs878853778
gwascentralrs878853778
openSNPrs878853778
23andMers878853778
23andMe allrs878853778
SNP Nexus

SNPshotrs878853778
SNPdbers878853778
MSV3drs878853778
GWAS Ctlgrs878853778
Max Magnitude0
ClinVar
Risk rs878853778(T;T)
Alt rs878853778(T;T)
Reference rs878853778(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37070321dupT
CLNSRC
CLNACC RCV000231982.1,