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rs386134123

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs386134123(C;C)
Make rs386134123(C;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position149210226
GeneCP
is asnp
is mentioned by
dbSNPrs386134123
ebirs386134123
HLIrs386134123
Exacrs386134123
Varsomers386134123
Maprs386134123
PheGenIrs386134123
hapmaprs386134123
1000 genomesrs386134123
hgdprs386134123
ensemblrs386134123
gopubmedrs386134123
geneviewrs386134123
scholarrs386134123
googlers386134123
pharmgkbrs386134123
gwascentralrs386134123
openSNPrs386134123
23andMers386134123
23andMe allrs386134123
SNP Nexus

SNPshotrs386134123
SNPdbers386134123
MSV3drs386134123
GWAS Ctlgrs386134123
Max Magnitude0
ClinVar
Risk rs386134123(C,G;C,G)
Alt rs386134123(C,G;C,G)
Reference rs386134123(T;T)
Significance Pathogenic
Disease Deficiency of ferroxidase
Variation info
Gene CP
CLNDBN Deficiency of ferroxidase
Reversed 1
HGVS NC_000003.11:g.148928013A>G
CLNSRC ClinVar GeneReviews
CLNACC RCV000034884.1,