Have questions? Visit https://www.reddit.com/r/SNPedia

rs199659114

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199659114(A;A)
Make rs199659114(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position855775
GeneELANE
is asnp
is mentioned by
dbSNPrs199659114
ebirs199659114
HLIrs199659114
Exacrs199659114
Varsomers199659114
Maprs199659114
PheGenIrs199659114
hapmaprs199659114
1000 genomesrs199659114
hgdprs199659114
ensemblrs199659114
gopubmedrs199659114
geneviewrs199659114
scholarrs199659114
googlers199659114
pharmgkbrs199659114
gwascentralrs199659114
openSNPrs199659114
23andMers199659114
23andMe allrs199659114
SNP Nexus

SNPshotrs199659114
SNPdbers199659114
MSV3drs199659114
GWAS Ctlgrs199659114
Max Magnitude0
ClinVar
Risk rs199659114(A;A)
Alt rs199659114(A;A)
Reference rs199659114(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene ELANE
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.855775G>A
CLNSRC
CLNACC RCV000227502.1,