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rs386134126

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs386134126(C;C)
Make rs386134126(C;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position149207551
GeneCP
is asnp
is mentioned by
dbSNPrs386134126
ebirs386134126
HLIrs386134126
Exacrs386134126
Varsomers386134126
Maprs386134126
PheGenIrs386134126
hapmaprs386134126
1000 genomesrs386134126
hgdprs386134126
ensemblrs386134126
gopubmedrs386134126
geneviewrs386134126
scholarrs386134126
googlers386134126
pharmgkbrs386134126
gwascentralrs386134126
openSNPrs386134126
23andMers386134126
23andMe allrs386134126
SNP Nexus

SNPshotrs386134126
SNPdbers386134126
MSV3drs386134126
GWAS Ctlgrs386134126
Max Magnitude0
ClinVar
Risk rs386134126(C;C)
Alt rs386134126(C;C)
Reference rs386134126(G;G)
Significance Pathogenic
Disease Deficiency of ferroxidase
Variation info
Gene CP
CLNDBN Deficiency of ferroxidase
Reversed 1
HGVS NC_000003.11:g.148925338C>G
CLNSRC ClinVar GeneReviews
CLNACC RCV000034953.1,