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rs386134137

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs386134137(A;G)
Make rs386134137(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position149202243
GeneCP
is asnp
is mentioned by
dbSNPrs386134137
ebirs386134137
HLIrs386134137
Exacrs386134137
Varsomers386134137
Maprs386134137
PheGenIrs386134137
hapmaprs386134137
1000 genomesrs386134137
hgdprs386134137
ensemblrs386134137
gopubmedrs386134137
geneviewrs386134137
scholarrs386134137
googlers386134137
pharmgkbrs386134137
gwascentralrs386134137
openSNPrs386134137
23andMers386134137
23andMe allrs386134137
SNP Nexus

SNPshotrs386134137
SNPdbers386134137
MSV3drs386134137
GWAS Ctlgrs386134137
Max Magnitude0
ClinVar
Risk rs386134137(G;G)
Alt rs386134137(G;G)
Reference rs386134137(A;A)
Significance Pathogenic
Disease Deficiency of ferroxidase
Variation info
Gene CP
CLNDBN Deficiency of ferroxidase
Reversed 1
HGVS NC_000003.11:g.148920030T>C
CLNSRC ClinVar GeneReviews
CLNACC RCV000034957.1,