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rs878853711

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GGTTG;GGTTG) 0 common in clinvar
Make rs878853711(CTTCTACCTCAAAAA;CTTCTACCTCAAAAA)
Make rs878853711(CTTCTACCTCAAAAA;GGTTG)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position47800039
GeneMSH6
is asnp
is mentioned by
dbSNPrs878853711
dbSNP (old)rs878853711
ClinGenrs878853711
ebirs878853711
HLIrs878853711
Exacrs878853711
Gnomadrs878853711
Varsomers878853711
Maprs878853711
PheGenIrs878853711
Biobankrs878853711
1000 genomesrs878853711
hgdprs878853711
ensemblrs878853711
gopubmedrs878853711
geneviewrs878853711
scholarrs878853711
googlers878853711
pharmgkbrs878853711
gwascentralrs878853711
openSNPrs878853711
23andMers878853711
23andMe allrs878853711
SNP Nexus

SNPshotrs878853711
SNPdbers878853711
MSV3drs878853711
GWAS Ctlgrs878853711
Max Magnitude0
ClinVar
Risk rs878853711(CTTCTACCTCAAAAA;CTTCTACCTCAAAAA)
Alt rs878853711(CTTCTACCTCAAAAA;CTTCTACCTCAAAAA)
Reference Rs878853711(GGTTG;GGTTG)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48027178_48027182delGGTTGinsCTTCTACCTCAAAAA
CLNSRC
CLNACC RCV000226342.2,