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rs587784326

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587784326(C;T)
Make rs587784326(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome22
Position38132850
GenePLA2G6
is asnp
is mentioned by
dbSNPrs587784326
ebirs587784326
HLIrs587784326
Exacrs587784326
Varsomers587784326
Maprs587784326
PheGenIrs587784326
hapmaprs587784326
1000 genomesrs587784326
hgdprs587784326
ensemblrs587784326
gopubmedrs587784326
geneviewrs587784326
scholarrs587784326
googlers587784326
pharmgkbrs587784326
gwascentralrs587784326
openSNPrs587784326
23andMers587784326
23andMe allrs587784326
SNP Nexus

SNPshotrs587784326
SNPdbers587784326
MSV3drs587784326
GWAS Ctlgrs587784326
Max Magnitude0
ClinVar
Risk rs587784326(T;T)
Alt rs587784326(T;T)
Reference rs587784326(C;C)
Significance Probable-Pathogenic
Disease Iron accumulation in brain
Variation info
Gene PLA2G6
CLNDBN Iron accumulation in brain
Reversed 1
HGVS NC_000022.10:g.38528857G>A
CLNSRC
CLNACC RCV000147280.1,