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rs386134135

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs386134135(A;A)
Make rs386134135(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position149210380
GeneCP
is asnp
is mentioned by
dbSNPrs386134135
ebirs386134135
HLIrs386134135
Exacrs386134135
Varsomers386134135
Maprs386134135
PheGenIrs386134135
hapmaprs386134135
1000 genomesrs386134135
hgdprs386134135
ensemblrs386134135
gopubmedrs386134135
geneviewrs386134135
scholarrs386134135
googlers386134135
pharmgkbrs386134135
gwascentralrs386134135
openSNPrs386134135
23andMers386134135
23andMe allrs386134135
SNP Nexus

SNPshotrs386134135
SNPdbers386134135
MSV3drs386134135
GWAS Ctlgrs386134135
Max Magnitude0
ClinVar
Risk rs386134135(A;A)
Alt rs386134135(A;A)
Reference rs386134135(G;G)
Significance Pathogenic
Disease Deficiency of ferroxidase
Variation info
Gene CP
CLNDBN Deficiency of ferroxidase
Reversed 1
HGVS NC_000003.11:g.148928167C>T
CLNSRC ClinVar GeneReviews
CLNACC RCV000034995.1,