rs9033
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs9033(C;C) |
Make rs9033(C;T) |
Make rs9033(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 16 |
Position | 67148096 |
Gene | B3GNT9, C16orf70 |
is a | snp |
is | mentioned by |
dbSNP | rs9033 |
dbSNP (classic) | rs9033 |
ClinGen | rs9033 |
ebi | rs9033 |
HLI | rs9033 |
Exac | rs9033 |
Gnomad | rs9033 |
Varsome | rs9033 |
LitVar | rs9033 |
Map | rs9033 |
PheGenI | rs9033 |
Biobank | rs9033 |
1000 genomes | rs9033 |
hgdp | rs9033 |
ensembl | rs9033 |
geneview | rs9033 |
scholar | rs9033 |
rs9033 | |
pharmgkb | rs9033 |
gwascentral | rs9033 |
openSNP | rs9033 |
23andMe | rs9033 |
SNPshot | rs9033 |
SNPdbe | rs9033 |
MSV3d | rs9033 |
GWAS Ctlg | rs9033 |
GMAF | 0.4417 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
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[PMID 19503744] An alphaA-crystallin gene mutation, Arg12Cys, causing inherited cataract-microcornea exhibits an altered heat-shock response.
[PMID 19668596] A novel gammaD-crystallin mutation causes mild changes in protein properties but leads to congenital coralliform cataract.