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rs386134146

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs386134146(-;-)
Make rs386134146(-;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position149186679
GeneCP
is asnp
is mentioned by
dbSNPrs386134146
ebirs386134146
HLIrs386134146
Exacrs386134146
Varsomers386134146
Maprs386134146
PheGenIrs386134146
hapmaprs386134146
1000 genomesrs386134146
hgdprs386134146
ensemblrs386134146
gopubmedrs386134146
geneviewrs386134146
scholarrs386134146
googlers386134146
pharmgkbrs386134146
gwascentralrs386134146
openSNPrs386134146
23andMers386134146
23andMe allrs386134146
SNP Nexus

SNPshotrs386134146
SNPdbers386134146
MSV3drs386134146
GWAS Ctlgrs386134146
Max Magnitude0
ClinVar
Risk rs386134146(;)
Alt rs386134146(;)
Reference rs386134146(G;G)
Significance Pathogenic
Disease Deficiency of ferroxidase
Variation info
Gene CP
CLNDBN Deficiency of ferroxidase
Reversed 1
HGVS NC_000003.11:g.148904466delC
CLNSRC ClinVar GeneReviews
CLNACC RCV000034968.2,