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rs121909579

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121909579(A;A)
Make rs121909579(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position149179587
GeneCP
is asnp
is mentioned by
dbSNPrs121909579
ebirs121909579
HLIrs121909579
Exacrs121909579
Varsomers121909579
Maprs121909579
PheGenIrs121909579
hapmaprs121909579
1000 genomesrs121909579
hgdprs121909579
ensemblrs121909579
gopubmedrs121909579
geneviewrs121909579
scholarrs121909579
googlers121909579
pharmgkbrs121909579
gwascentralrs121909579
openSNPrs121909579
23andMers121909579
23andMe allrs121909579
SNP Nexus

SNPshotrs121909579
SNPdbers121909579
MSV3drs121909579
GWAS Ctlgrs121909579
Max Magnitude0
OMIM117700
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121909579(A;A)
Alt rs121909579(A;A)
Reference rs121909579(G;G)
Significance Pathogenic
Disease Deficiency of ferroxidase Hypoceruloplasminemia
Variation info
Gene CP
CLNDBN Deficiency of ferroxidase Hypoceruloplasminemia
Reversed 1
HGVS NC_000003.11:g.148897374C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000019120.37, RCV000019121.27,