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rs1064797073

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome3
Position149198401
GeneCP
is asnp
is mentioned by
dbSNPrs1064797073
dbSNP (classic)rs1064797073
ClinGenrs1064797073
ebirs1064797073
HLIrs1064797073
Exacrs1064797073
Gnomadrs1064797073
Varsomers1064797073
LitVarrs1064797073
Maprs1064797073
PheGenIrs1064797073
Biobankrs1064797073
1000 genomesrs1064797073
hgdprs1064797073
ensemblrs1064797073
geneviewrs1064797073
scholarrs1064797073
googlers1064797073
pharmgkbrs1064797073
gwascentralrs1064797073
openSNPrs1064797073
23andMers1064797073
23andMe allrs1064797073
SNPshotrs1064797073
SNPdbers1064797073
MSV3drs1064797073
GWAS Ctlgrs1064797073
Max Magnitude0
ClinVar
Risk rs1064797073(T;T)
Alt rs1064797073(T;T)
Reference Rs1064797073(G;G)
Significance Probable-Pathogenic
Disease Deficiency of ferroxidase
Variation info
Gene CP
CLNDBN Deficiency of ferroxidase
Reversed 1
HGVS NC_000003.11:g.148916188C>A
CLNSRC
CLNACC RCV000487430.1,