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

rs876658296

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GGCCCAGGCCCTT;GGCCCAGGCCCTT) 0 common in clinvar
Make rs876658296(-;-)
Make rs876658296(-;CCAGGCCCTTGGC)
Make rs876658296(CCAGGCCCTTGGC;CCAGGCCCTTGGC)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position47783403
GeneMSH6
is asnp
is mentioned by
dbSNPrs876658296
dbSNP (old)rs876658296
ClinGenrs876658296
ebirs876658296
HLIrs876658296
Exacrs876658296
Gnomadrs876658296
Varsomers876658296
Maprs876658296
PheGenIrs876658296
Biobankrs876658296
1000 genomesrs876658296
hgdprs876658296
ensemblrs876658296
gopubmedrs876658296
geneviewrs876658296
scholarrs876658296
googlers876658296
pharmgkbrs876658296
gwascentralrs876658296
openSNPrs876658296
23andMers876658296
23andMe allrs876658296
SNP Nexus

SNPshotrs876658296
SNPdbers876658296
MSV3drs876658296
GWAS Ctlgrs876658296
Max Magnitude0
ClinVar
Risk rs876658296(-;-)
Alt rs876658296(-;-)
Reference Rs876658296(GGCCCAGGCCCTT;GGCCCAGGCCCTT)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MSH6
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.48010542_48010554delCCAGGCCCTTGGC
CLNSRC
CLNACC RCV000215541.1,