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rs878855318

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878855318(A;A)
Make rs878855318(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position855795
GeneELANE
is asnp
is mentioned by
dbSNPrs878855318
ebirs878855318
HLIrs878855318
Exacrs878855318
Varsomers878855318
Maprs878855318
PheGenIrs878855318
hapmaprs878855318
1000 genomesrs878855318
hgdprs878855318
ensemblrs878855318
gopubmedrs878855318
geneviewrs878855318
scholarrs878855318
googlers878855318
pharmgkbrs878855318
gwascentralrs878855318
openSNPrs878855318
23andMers878855318
23andMe allrs878855318
SNP Nexus

SNPshotrs878855318
SNPdbers878855318
MSV3drs878855318
GWAS Ctlgrs878855318
Max Magnitude0
ClinVar
Risk rs878855318(A;A)
Alt rs878855318(A;A)
Reference rs878855318(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene ELANE
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.855795G>A; NC_000019.9:g.855795G>C
CLNSRC
CLNACC RCV000229570.1, RCV000237098.1,