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rs878855317

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878855317(A;A)
Make rs878855317(A;C)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position855755
GeneELANE
is asnp
is mentioned by
dbSNPrs878855317
ebirs878855317
HLIrs878855317
Exacrs878855317
Varsomers878855317
Maprs878855317
PheGenIrs878855317
hapmaprs878855317
1000 genomesrs878855317
hgdprs878855317
ensemblrs878855317
gopubmedrs878855317
geneviewrs878855317
scholarrs878855317
googlers878855317
pharmgkbrs878855317
gwascentralrs878855317
openSNPrs878855317
23andMers878855317
23andMe allrs878855317
SNP Nexus

SNPshotrs878855317
SNPdbers878855317
MSV3drs878855317
GWAS Ctlgrs878855317
Max Magnitude0
ClinVar
Risk rs878855317(A;A)
Alt rs878855317(A;A)
Reference rs878855317(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene ELANE
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.855755C>A
CLNSRC
CLNACC RCV000226863.1,