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rs879253882

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs879253882(A;A)
Make rs879253882(A;G)
ReferenceGRCh38.p7 38.3/149
Chromosome19
Position855799
GeneELANE
is asnp
is mentioned by
dbSNPrs879253882
dbSNP (classic)rs879253882
ClinGenrs879253882
ebirs879253882
HLIrs879253882
Exacrs879253882
Gnomadrs879253882
Varsomers879253882
LitVarrs879253882
Maprs879253882
PheGenIrs879253882
Biobankrs879253882
1000 genomesrs879253882
hgdprs879253882
ensemblrs879253882
geneviewrs879253882
scholarrs879253882
googlers879253882
pharmgkbrs879253882
gwascentralrs879253882
openSNPrs879253882
23andMers879253882
23andMe allrs879253882
SNPshotrs879253882
SNPdbers879253882
MSV3drs879253882
GWAS Ctlgrs879253882
Max Magnitude0
ClinVar
Risk rs879253882(A;A)
Alt rs879253882(A;A)
Reference Rs879253882(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene ELANE
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.855799G>A
CLNSRC
CLNACC RCV000236267.1,