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rs200683433

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs200683433(C;G)
Make rs200683433(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position149212616
GeneCP
is asnp
is mentioned by
dbSNPrs200683433
ebirs200683433
HLIrs200683433
Exacrs200683433
Varsomers200683433
Maprs200683433
PheGenIrs200683433
hapmaprs200683433
1000 genomesrs200683433
hgdprs200683433
ensemblrs200683433
gopubmedrs200683433
geneviewrs200683433
scholarrs200683433
googlers200683433
pharmgkbrs200683433
gwascentralrs200683433
openSNPrs200683433
23andMers200683433
23andMe allrs200683433
SNP Nexus

SNPshotrs200683433
SNPdbers200683433
MSV3drs200683433
GWAS Ctlgrs200683433
Max Magnitude0
ClinVar
Risk rs200683433(G;G)
Alt rs200683433(G;G)
Reference rs200683433(C;C)
Significance Pathogenic
Disease Deficiency of ferroxidase
Variation info
Gene CP
CLNDBN Deficiency of ferroxidase
Reversed 0
HGVS NC_000003.11:g.148930403C>G
CLNSRC ClinVar GeneReviews
CLNACC RCV000034878.1,