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rs386134147

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs386134147(-;-)
Make rs386134147(-;C)
ReferenceGRCh38 38.1/141
Chromosome3
Position149186532
GeneCP
is asnp
is mentioned by
dbSNPrs386134147
ebirs386134147
HLIrs386134147
Exacrs386134147
Varsomers386134147
Maprs386134147
PheGenIrs386134147
hapmaprs386134147
1000 genomesrs386134147
hgdprs386134147
ensemblrs386134147
gopubmedrs386134147
geneviewrs386134147
scholarrs386134147
googlers386134147
pharmgkbrs386134147
gwascentralrs386134147
openSNPrs386134147
23andMers386134147
23andMe allrs386134147
SNP Nexus

SNPshotrs386134147
SNPdbers386134147
MSV3drs386134147
GWAS Ctlgrs386134147
Max Magnitude0
ClinVar
Risk rs386134147(;)
Alt rs386134147(;)
Reference rs386134147(C;C)
Significance Pathogenic
Disease Deficiency of ferroxidase
Variation info
Gene CP
CLNDBN Deficiency of ferroxidase
Reversed 1
HGVS NC_000003.11:g.148904319delG
CLNSRC ClinVar GeneReviews
CLNACC RCV000034970.2,