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rs386134129

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs386134129(A;A)
Make rs386134129(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position149186723
GeneCP
is asnp
is mentioned by
dbSNPrs386134129
ebirs386134129
HLIrs386134129
Exacrs386134129
Varsomers386134129
Maprs386134129
PheGenIrs386134129
hapmaprs386134129
1000 genomesrs386134129
hgdprs386134129
ensemblrs386134129
gopubmedrs386134129
geneviewrs386134129
scholarrs386134129
googlers386134129
pharmgkbrs386134129
gwascentralrs386134129
openSNPrs386134129
23andMers386134129
23andMe allrs386134129
SNP Nexus

SNPshotrs386134129
SNPdbers386134129
MSV3drs386134129
GWAS Ctlgrs386134129
Max Magnitude0
ClinVar
Risk rs386134129(A;A)
Alt rs386134129(A;A)
Reference rs386134129(G;G)
Significance Pathogenic
Disease Deficiency of ferroxidase
Variation info
Gene CP
CLNDBN Deficiency of ferroxidase
Reversed 1
HGVS NC_000003.11:g.148904510C>T
CLNSRC ClinVar GeneReviews
CLNACC RCV000034880.1,