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rs878855323

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs878855323(-;CCATAACCTCTC)
Make rs878855323(CCATAACCTCTC;CCATAACCTCTC)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position853306
GeneELANE
is asnp
is mentioned by
dbSNPrs878855323
dbSNP (classic)rs878855323
ClinGenrs878855323
ebirs878855323
HLIrs878855323
Exacrs878855323
Gnomadrs878855323
Varsomers878855323
LitVarrs878855323
Maprs878855323
PheGenIrs878855323
Biobankrs878855323
1000 genomesrs878855323
hgdprs878855323
ensemblrs878855323
geneviewrs878855323
scholarrs878855323
googlers878855323
pharmgkbrs878855323
gwascentralrs878855323
openSNPrs878855323
23andMers878855323
SNPshotrs878855323
SNPdbers878855323
MSV3drs878855323
GWAS Ctlgrs878855323
Max Magnitude0
ClinVar
Risk rs878855323(CCATAACCTCTC;CCATAACCTCTC) rs878855323(CCCATAACCTCT;CCCATAACCTCT)
Alt rs878855323(CCATAACCTCTC;CCATAACCTCTC) rs878855323(CCCATAACCTCT;CCCATAACCTCT)
Reference Rs878855323(-;-)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ELANE
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.853295_853306dupCCATAACCTCTC
CLNSRC
CLNACC RCV000226787.1,