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rs386134152

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs386134152(-;-)
Make rs386134152(-;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position149179615
GeneCP
is asnp
is mentioned by
dbSNPrs386134152
ebirs386134152
HLIrs386134152
Exacrs386134152
Varsomers386134152
Maprs386134152
PheGenIrs386134152
hapmaprs386134152
1000 genomesrs386134152
hgdprs386134152
ensemblrs386134152
gopubmedrs386134152
geneviewrs386134152
scholarrs386134152
googlers386134152
pharmgkbrs386134152
gwascentralrs386134152
openSNPrs386134152
23andMers386134152
23andMe allrs386134152
SNP Nexus

SNPshotrs386134152
SNPdbers386134152
MSV3drs386134152
GWAS Ctlgrs386134152
Max Magnitude0
ClinVar
Risk rs386134152(;)
Alt rs386134152(;)
Reference rs386134152(G;G)
Significance Pathogenic
Disease Deficiency of ferroxidase
Variation info
Gene CP
CLNDBN Deficiency of ferroxidase
Reversed 1
HGVS NC_000003.11:g.148897402delC
CLNSRC ClinVar GeneReviews
CLNACC RCV000034980.2,