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

rs587777923

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587777923(-;-)
Make rs587777923(-;T)
Make rs587777923(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position149182047
GeneCP
is asnp
is mentioned by
dbSNPrs587777923
ebirs587777923
HLIrs587777923
Exacrs587777923
Varsomers587777923
Maprs587777923
PheGenIrs587777923
hapmaprs587777923
1000 genomesrs587777923
hgdprs587777923
ensemblrs587777923
gopubmedrs587777923
geneviewrs587777923
scholarrs587777923
googlers587777923
pharmgkbrs587777923
gwascentralrs587777923
openSNPrs587777923
23andMers587777923
23andMe allrs587777923
SNP Nexus

SNPshotrs587777923
SNPdbers587777923
MSV3drs587777923
GWAS Ctlgrs587777923
Max Magnitude0
ClinVar
Risk rs587777923(T;T)
Alt rs587777923(T;T)
Reference rs587777923(;)
Significance Pathogenic
Disease Deficiency of ferroxidase
Variation info
Gene CP
CLNDBN Deficiency of ferroxidase
Reversed 1
HGVS NC_000003.11:g.148899835dupA
CLNSRC
CLNACC RCV000034978.1,