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rs386134156

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs386134156(C;T)
Make rs386134156(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position149178592
GeneCP
is asnp
is mentioned by
dbSNPrs386134156
ebirs386134156
HLIrs386134156
Exacrs386134156
Varsomers386134156
Maprs386134156
PheGenIrs386134156
hapmaprs386134156
1000 genomesrs386134156
hgdprs386134156
ensemblrs386134156
gopubmedrs386134156
geneviewrs386134156
scholarrs386134156
googlers386134156
pharmgkbrs386134156
gwascentralrs386134156
openSNPrs386134156
23andMers386134156
23andMe allrs386134156
SNP Nexus

SNPshotrs386134156
SNPdbers386134156
MSV3drs386134156
GWAS Ctlgrs386134156
Max Magnitude0
ClinVar
Risk rs386134156(T;T)
Alt rs386134156(T;T)
Reference rs386134156(C;C)
Significance Pathogenic
Disease Deficiency of ferroxidase
Variation info
Gene CP
CLNDBN Deficiency of ferroxidase
Reversed 1
HGVS NC_000003.11:g.148896379G>A
CLNSRC ClinVar GeneReviews
CLNACC RCV000034951.2,