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

rs587777922

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587777922(-;-)
Make rs587777922(-;C)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position149185339
GeneCP
is asnp
is mentioned by
dbSNPrs587777922
ebirs587777922
HLIrs587777922
Exacrs587777922
Varsomers587777922
Maprs587777922
PheGenIrs587777922
hapmaprs587777922
1000 genomesrs587777922
hgdprs587777922
ensemblrs587777922
gopubmedrs587777922
geneviewrs587777922
scholarrs587777922
googlers587777922
pharmgkbrs587777922
gwascentralrs587777922
openSNPrs587777922
23andMers587777922
23andMe allrs587777922
SNP Nexus

SNPshotrs587777922
SNPdbers587777922
MSV3drs587777922
GWAS Ctlgrs587777922
Max Magnitude0
ClinVar
Risk rs587777922(;)
Alt rs587777922(;)
Reference rs587777922(C;C)
Significance Pathogenic
Disease Deficiency of ferroxidase
Variation info
Gene CP
CLNDBN Deficiency of ferroxidase
Reversed 1
HGVS NC_000003.11:g.148903126delG
CLNSRC
CLNACC RCV000034974.1,