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rs386134122

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs386134122(C;G)
Make rs386134122(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position149210281
GeneCP
is asnp
is mentioned by
dbSNPrs386134122
ebirs386134122
HLIrs386134122
Exacrs386134122
Varsomers386134122
Maprs386134122
PheGenIrs386134122
hapmaprs386134122
1000 genomesrs386134122
hgdprs386134122
ensemblrs386134122
gopubmedrs386134122
geneviewrs386134122
scholarrs386134122
googlers386134122
pharmgkbrs386134122
gwascentralrs386134122
openSNPrs386134122
23andMers386134122
23andMe allrs386134122
SNP Nexus

SNPshotrs386134122
SNPdbers386134122
MSV3drs386134122
GWAS Ctlgrs386134122
Max Magnitude0
ClinVar
Risk rs386134122(G;G)
Alt rs386134122(G;G)
Reference rs386134122(C;C)
Significance Pathogenic
Disease Deficiency of ferroxidase
Variation info
Gene CP
CLNDBN Deficiency of ferroxidase
Reversed 1
HGVS NC_000003.11:g.148928068G>C
CLNSRC ClinVar GeneReviews
CLNACC RCV000034947.1,