Have questions? Visit https://www.reddit.com/r/SNPedia

rs386134144

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TT;TT) 0 common in clinvar
Make rs386134144(-;-)
Make rs386134144(-;TT)
ReferenceGRCh38 38.1/141
Chromosome3
Position149202192
GeneCP
is asnp
is mentioned by
dbSNPrs386134144
ebirs386134144
HLIrs386134144
Exacrs386134144
Varsomers386134144
Maprs386134144
PheGenIrs386134144
hapmaprs386134144
1000 genomesrs386134144
hgdprs386134144
ensemblrs386134144
gopubmedrs386134144
geneviewrs386134144
scholarrs386134144
googlers386134144
pharmgkbrs386134144
gwascentralrs386134144
openSNPrs386134144
23andMers386134144
23andMe allrs386134144
SNP Nexus

SNPshotrs386134144
SNPdbers386134144
MSV3drs386134144
GWAS Ctlgrs386134144
Max Magnitude0
ClinVar
Risk rs386134144(;)
Alt rs386134144(;)
Reference rs386134144(TT;TT)
Significance Pathogenic
Disease Deficiency of ferroxidase
Variation info
Gene CP
CLNDBN Deficiency of ferroxidase
Reversed 1
HGVS NC_000003.11:g.148919979_148919980delAA
CLNSRC ClinVar GeneReviews
CLNACC RCV000034960.2,