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rs878853736

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs878853736(-;-)
Make rs878853736(-;AAAAT)
Make rs878853736(AAAAT;AAAAT)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position47806278
GeneMSH6
is asnp
is mentioned by
dbSNPrs878853736
ebirs878853736
HLIrs878853736
Exacrs878853736
Varsomers878853736
Maprs878853736
PheGenIrs878853736
hapmaprs878853736
1000 genomesrs878853736
hgdprs878853736
ensemblrs878853736
gopubmedrs878853736
geneviewrs878853736
scholarrs878853736
googlers878853736
pharmgkbrs878853736
gwascentralrs878853736
openSNPrs878853736
23andMers878853736
23andMe allrs878853736
SNP Nexus

SNPshotrs878853736
SNPdbers878853736
MSV3drs878853736
GWAS Ctlgrs878853736
Max Magnitude0
ClinVar
Risk rs878853736(ATAAA;ATAAA)
Alt rs878853736(ATAAA;ATAAA)
Reference rs878853736(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48033413_48033417dupAAAAT
CLNSRC
CLNACC RCV000232271.1,