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rs878853785

From SNPedia

Orientationplus
Geno Mag Summary
(TA;TA) 0 common in clinvar
Make rs878853785(-;-)
Make rs878853785(-;AT)
Make rs878853785(AT;AT)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position37048958
GeneMLH1
is asnp
is mentioned by
dbSNPrs878853785
ebirs878853785
HLIrs878853785
Exacrs878853785
Varsomers878853785
Maprs878853785
PheGenIrs878853785
hapmaprs878853785
1000 genomesrs878853785
hgdprs878853785
ensemblrs878853785
gopubmedrs878853785
geneviewrs878853785
scholarrs878853785
googlers878853785
pharmgkbrs878853785
gwascentralrs878853785
openSNPrs878853785
23andMers878853785
23andMe allrs878853785
SNP Nexus

SNPshotrs878853785
SNPdbers878853785
MSV3drs878853785
GWAS Ctlgrs878853785
Max Magnitude0
ClinVar
Risk rs878853785(;)
Alt rs878853785(;)
Reference rs878853785(TA;TA)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MLH1
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000003.11:g.37090449_37090450delAT
CLNSRC
CLNACC RCV000232267.1,