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rs386134155

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs386134155(C;T)
Make rs386134155(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position149209349
GeneCP
is asnp
is mentioned by
dbSNPrs386134155
ebirs386134155
HLIrs386134155
Exacrs386134155
Varsomers386134155
Maprs386134155
PheGenIrs386134155
hapmaprs386134155
1000 genomesrs386134155
hgdprs386134155
ensemblrs386134155
gopubmedrs386134155
geneviewrs386134155
scholarrs386134155
googlers386134155
pharmgkbrs386134155
gwascentralrs386134155
openSNPrs386134155
23andMers386134155
23andMe allrs386134155
SNP Nexus

SNPshotrs386134155
SNPdbers386134155
MSV3drs386134155
GWAS Ctlgrs386134155
Max Magnitude0
ClinVar
Risk rs386134155(T;T)
Alt rs386134155(T;T)
Reference rs386134155(C;C)
Significance Pathogenic
Disease Deficiency of ferroxidase
Variation info
Gene CP
CLNDBN Deficiency of ferroxidase
Reversed 1
HGVS NC_000003.11:g.148927136G>A
CLNSRC ClinVar GeneReviews
CLNACC RCV000034949.2,