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rs386134151

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs386134151(-;-)
Make rs386134151(-;T)
Make rs386134151(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position149182048
GeneCP
is asnp
is mentioned by
dbSNPrs386134151
ebirs386134151
HLIrs386134151
Exacrs386134151
Varsomers386134151
Maprs386134151
PheGenIrs386134151
hapmaprs386134151
1000 genomesrs386134151
hgdprs386134151
ensemblrs386134151
gopubmedrs386134151
geneviewrs386134151
scholarrs386134151
googlers386134151
pharmgkbrs386134151
gwascentralrs386134151
openSNPrs386134151
23andMers386134151
23andMe allrs386134151
SNP Nexus

SNPshotrs386134151
SNPdbers386134151
MSV3drs386134151
GWAS Ctlgrs386134151
Max Magnitude0
ClinVar
Risk rs386134151(T;T)
Alt rs386134151(T;T)
Reference rs386134151(;)
Significance Pathogenic
Disease Deficiency of ferroxidase
Variation info
Gene CP
CLNDBN Deficiency of ferroxidase
Reversed 1
HGVS NC_000003.11:g.148899835dupA
CLNSRC ClinVar GeneReviews
CLNACC RCV000034978.1,