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rs878855321

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878855321(C;T)
Make rs878855321(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position855965
GeneELANE
is asnp
is mentioned by
dbSNPrs878855321
ebirs878855321
HLIrs878855321
Exacrs878855321
Varsomers878855321
Maprs878855321
PheGenIrs878855321
hapmaprs878855321
1000 genomesrs878855321
hgdprs878855321
ensemblrs878855321
gopubmedrs878855321
geneviewrs878855321
scholarrs878855321
googlers878855321
pharmgkbrs878855321
gwascentralrs878855321
openSNPrs878855321
23andMers878855321
23andMe allrs878855321
SNP Nexus

SNPshotrs878855321
SNPdbers878855321
MSV3drs878855321
GWAS Ctlgrs878855321
Max Magnitude0
ClinVar
Risk rs878855321(T;T)
Alt rs878855321(T;T)
Reference rs878855321(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ELANE
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.855965C>T
CLNSRC
CLNACC RCV000228433.1,