rs7144
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs7144(C;C) |
Make rs7144(C;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 207794374 |
Gene | CD46 |
is a | snp |
is | mentioned by |
dbSNP | rs7144 |
dbSNP (classic) | rs7144 |
ClinGen | rs7144 |
ebi | rs7144 |
HLI | rs7144 |
Exac | rs7144 |
Gnomad | rs7144 |
Varsome | rs7144 |
LitVar | rs7144 |
Map | rs7144 |
PheGenI | rs7144 |
Biobank | rs7144 |
1000 genomes | rs7144 |
hgdp | rs7144 |
ensembl | rs7144 |
geneview | rs7144 |
scholar | rs7144 |
rs7144 | |
pharmgkb | rs7144 |
gwascentral | rs7144 |
openSNP | rs7144 |
23andMe | rs7144 |
SNPshot | rs7144 |
SNPdbe | rs7144 |
MSV3d | rs7144 |
GWAS Ctlg | rs7144 |
GMAF | 0.3563 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 22357652] CD46 measles receptor polymorphisms influence receptor protein expression and primary measles vaccine responses in naive Australian children
[PMID 18483746] Plasma therapy in atypical haemolytic uremic syndrome: lessons from a family with a factor H mutation.
[PMID 19861685] Association of factor H autoantibodies with deletions of CFHR1, CFHR3, CFHR4, and with mutations in CFH, CFI, CD46, and C3 in patients with atypical hemolytic uremic syndrome.
ClinVar | |
---|---|
Risk | rs7144(C;C) |
Alt | rs7144(C;C) |
Reference | Rs7144(T;T) |
Significance | Non-pathogenic |
Disease | Atypical hemolytic uremic syndrome |
Variation | info |
Gene | CD46 |
CLNDBN | Atypical hemolytic uremic syndrome |
Reversed | 0 |
HGVS | NC_000001.10:g.207967719T>C |
CLNSRC | |
CLNACC | RCV000385547.1, |