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rs878855319

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs878855319(C;C)
Make rs878855319(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position852948
GeneELANE
is asnp
is mentioned by
dbSNPrs878855319
ebirs878855319
HLIrs878855319
Exacrs878855319
Varsomers878855319
Maprs878855319
PheGenIrs878855319
hapmaprs878855319
1000 genomesrs878855319
hgdprs878855319
ensemblrs878855319
gopubmedrs878855319
geneviewrs878855319
scholarrs878855319
googlers878855319
pharmgkbrs878855319
gwascentralrs878855319
openSNPrs878855319
23andMers878855319
23andMe allrs878855319
SNP Nexus

SNPshotrs878855319
SNPdbers878855319
MSV3drs878855319
GWAS Ctlgrs878855319
Max Magnitude0
ClinVar
Risk rs878855319(C;C)
Alt rs878855319(C;C)
Reference rs878855319(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene ELANE
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.852948T>C
CLNSRC
CLNACC RCV000225846.1,