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rs701753

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
(T;T) 0 common in clinvar
Make rs701753(A;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position149198448
GeneCP
is asnp
is mentioned by
dbSNPrs701753
dbSNP (classic)rs701753
ClinGenrs701753
ebirs701753
HLIrs701753
Exacrs701753
Gnomadrs701753
Varsomers701753
LitVarrs701753
Maprs701753
PheGenIrs701753
Biobankrs701753
1000 genomesrs701753
hgdprs701753
ensemblrs701753
geneviewrs701753
scholarrs701753
googlers701753
pharmgkbrs701753
gwascentralrs701753
openSNPrs701753
23andMers701753
SNPshotrs701753
SNPdbers701753
MSV3drs701753
GWAS Ctlgrs701753
GMAF0.1139
Max Magnitude0
? (A;A) (A;T) (T;T) 28



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[PMID 25943368OA-icon.png] Ceruloplasmin activity and iron chelation treatment of patients with Parkinson's disease


ClinVar
Risk Rs701753(A;A)
Alt Rs701753(A;A)
Reference Rs701753(T;T)
Significance Non-pathogenic
Disease not specified
Variation info
Gene CP
CLNDBN not specified
Reversed 0
HGVS NC_000003.11:g.148916235T>A
CLNSRC
CLNACC RCV000180465.1,