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rs878855326

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878855326(A;A)
Make rs878855326(A;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position49075659
GenePRAF2, WDR45
is asnp
is mentioned by
dbSNPrs878855326
ebirs878855326
HLIrs878855326
Exacrs878855326
Varsomers878855326
Maprs878855326
PheGenIrs878855326
hapmaprs878855326
1000 genomesrs878855326
hgdprs878855326
ensemblrs878855326
gopubmedrs878855326
geneviewrs878855326
scholarrs878855326
googlers878855326
pharmgkbrs878855326
gwascentralrs878855326
openSNPrs878855326
23andMers878855326
23andMe allrs878855326
SNP Nexus

SNPshotrs878855326
SNPdbers878855326
MSV3drs878855326
GWAS Ctlgrs878855326
Max Magnitude0
ClinVar
Risk rs878855326(A;A)
Alt rs878855326(A;A)
Reference rs878855326(G;G)
Significance Pathogenic
Disease Neurodegeneration with brain iron accumulation 5
Variation info
Gene WDR45 PRAF2
CLNDBN Neurodegeneration with brain iron accumulation 5
Reversed 1
HGVS NC_000023.10:g.48933318C>T
CLNSRC
CLNACC RCV000234791.1,