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rs386134141

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs386134141(A;A)
Make rs386134141(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position149177980
GeneCP
is asnp
is mentioned by
dbSNPrs386134141
ebirs386134141
HLIrs386134141
Exacrs386134141
Varsomers386134141
Maprs386134141
PheGenIrs386134141
hapmaprs386134141
1000 genomesrs386134141
hgdprs386134141
ensemblrs386134141
gopubmedrs386134141
geneviewrs386134141
scholarrs386134141
googlers386134141
pharmgkbrs386134141
gwascentralrs386134141
openSNPrs386134141
23andMers386134141
23andMe allrs386134141
SNP Nexus

SNPshotrs386134141
SNPdbers386134141
MSV3drs386134141
GWAS Ctlgrs386134141
Max Magnitude0
ClinVar
Risk rs386134141(A;A)
Alt rs386134141(A;A)
Reference rs386134141(G;G)
Significance Pathogenic
Disease Deficiency of ferroxidase
Variation info
Gene CP
CLNDBN Deficiency of ferroxidase
Reversed 1
HGVS NC_000003.11:g.148895767C>T
CLNSRC ClinVar GeneReviews
CLNACC RCV000034982.2,