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rs587784331

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587784331(C;T)
Make rs587784331(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome22
Position38123197
GenePLA2G6
is asnp
is mentioned by
dbSNPrs587784331
ebirs587784331
HLIrs587784331
Exacrs587784331
Varsomers587784331
Maprs587784331
PheGenIrs587784331
hapmaprs587784331
1000 genomesrs587784331
hgdprs587784331
ensemblrs587784331
gopubmedrs587784331
geneviewrs587784331
scholarrs587784331
googlers587784331
pharmgkbrs587784331
gwascentralrs587784331
openSNPrs587784331
23andMers587784331
23andMe allrs587784331
SNP Nexus

SNPshotrs587784331
SNPdbers587784331
MSV3drs587784331
GWAS Ctlgrs587784331
Max Magnitude0
ClinVar
Risk rs587784331(T;T)
Alt rs587784331(T;T)
Reference rs587784331(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.38519204G>A
CLNSRC
CLNACC RCV000147287.1,