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rs878853702

From SNPedia

Orientationplus
Geno Mag Summary
(TA;TA) 0 common in clinvar
Make rs878853702(-;-)
Make rs878853702(-;AT)
Make rs878853702(AT;AT)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position47799333
GeneMSH6
is asnp
is mentioned by
dbSNPrs878853702
ebirs878853702
HLIrs878853702
Exacrs878853702
Varsomers878853702
Maprs878853702
PheGenIrs878853702
hapmaprs878853702
1000 genomesrs878853702
hgdprs878853702
ensemblrs878853702
gopubmedrs878853702
geneviewrs878853702
scholarrs878853702
googlers878853702
pharmgkbrs878853702
gwascentralrs878853702
openSNPrs878853702
23andMers878853702
23andMe allrs878853702
SNP Nexus

SNPshotrs878853702
SNPdbers878853702
MSV3drs878853702
GWAS Ctlgrs878853702
Max Magnitude0
ClinVar
Risk rs878853702(;)
Alt rs878853702(;)
Reference rs878853702(TA;TA)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48026472_48026473delAT
CLNSRC
CLNACC RCV000228751.1,