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rs386134136

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs386134136(A;A)
Make rs386134136(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position149210166
GeneCP
is asnp
is mentioned by
dbSNPrs386134136
ebirs386134136
HLIrs386134136
Exacrs386134136
Varsomers386134136
Maprs386134136
PheGenIrs386134136
hapmaprs386134136
1000 genomesrs386134136
hgdprs386134136
ensemblrs386134136
gopubmedrs386134136
geneviewrs386134136
scholarrs386134136
googlers386134136
pharmgkbrs386134136
gwascentralrs386134136
openSNPrs386134136
23andMers386134136
23andMe allrs386134136
SNP Nexus

SNPshotrs386134136
SNPdbers386134136
MSV3drs386134136
GWAS Ctlgrs386134136
Max Magnitude0
ClinVar
Risk rs386134136(A;A)
Alt rs386134136(A;A)
Reference rs386134136(G;G)
Significance Pathogenic
Disease Deficiency of ferroxidase
Variation info
Gene CP
CLNDBN Deficiency of ferroxidase
Reversed 1
HGVS NC_000003.11:g.148927953C>T
CLNSRC ClinVar GeneReviews
CLNACC RCV000035000.1,