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rs587784364

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587784364(C;C)
Make rs587784364(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome22
Position38132914
GenePLA2G6
is asnp
is mentioned by
dbSNPrs587784364
ebirs587784364
HLIrs587784364
Exacrs587784364
Varsomers587784364
Maprs587784364
PheGenIrs587784364
hapmaprs587784364
1000 genomesrs587784364
hgdprs587784364
ensemblrs587784364
gopubmedrs587784364
geneviewrs587784364
scholarrs587784364
googlers587784364
pharmgkbrs587784364
gwascentralrs587784364
openSNPrs587784364
23andMers587784364
23andMe allrs587784364
SNP Nexus

SNPshotrs587784364
SNPdbers587784364
MSV3drs587784364
GWAS Ctlgrs587784364
Max Magnitude0
ClinVar
Risk rs587784364(C;C)
Alt rs587784364(C;C)
Reference rs587784364(T;T)
Significance Probable-Pathogenic
Disease Iron accumulation in brain
Variation info
Gene PLA2G6
CLNDBN Iron accumulation in brain
Reversed 1
HGVS NC_000022.10:g.38528921A>G
CLNSRC
CLNACC RCV000147341.1,