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rs386134132

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs386134132(A;G)
Make rs386134132(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position149177905
GeneCP
is asnp
is mentioned by
dbSNPrs386134132
ebirs386134132
HLIrs386134132
Exacrs386134132
Varsomers386134132
Maprs386134132
PheGenIrs386134132
hapmaprs386134132
1000 genomesrs386134132
hgdprs386134132
ensemblrs386134132
gopubmedrs386134132
geneviewrs386134132
scholarrs386134132
googlers386134132
pharmgkbrs386134132
gwascentralrs386134132
openSNPrs386134132
23andMers386134132
23andMe allrs386134132
SNP Nexus

SNPshotrs386134132
SNPdbers386134132
MSV3drs386134132
GWAS Ctlgrs386134132
Max Magnitude0
ClinVar
Risk rs386134132(G;G)
Alt rs386134132(G;G)
Reference rs386134132(A;A)
Significance Pathogenic
Disease Deficiency of ferroxidase
Variation info
Gene CP
CLNDBN Deficiency of ferroxidase
Reversed 1
HGVS NC_000003.11:g.148895692T>C
CLNSRC ClinVar GeneReviews
CLNACC RCV000034888.1,