rs701753
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in complete genomics |
(T;T) | 0 | common in clinvar |
Make rs701753(A;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 149198448 |
Gene | CP |
is a | snp |
is | mentioned by |
dbSNP | rs701753 |
dbSNP (classic) | rs701753 |
ClinGen | rs701753 |
ebi | rs701753 |
HLI | rs701753 |
Exac | rs701753 |
Gnomad | rs701753 |
Varsome | rs701753 |
LitVar | rs701753 |
Map | rs701753 |
PheGenI | rs701753 |
Biobank | rs701753 |
1000 genomes | rs701753 |
hgdp | rs701753 |
ensembl | rs701753 |
geneview | rs701753 |
scholar | rs701753 |
rs701753 | |
pharmgkb | rs701753 |
gwascentral | rs701753 |
openSNP | rs701753 |
23andMe | rs701753 |
SNPshot | rs701753 |
SNPdbe | rs701753 |
MSV3d | rs701753 |
GWAS Ctlg | rs701753 |
GMAF | 0.1139 |
Max Magnitude | 0 |
? | (A;A) (A;T) (T;T) | 28 |
---|---|---|
|
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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, |