rs245111
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs245111(C;C) |
Make rs245111(C;T) |
Make rs245111(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 19 |
Position | 50025640 |
Gene | VRK3, ZNF473 |
is a | snp |
is | mentioned by |
dbSNP | rs245111 |
dbSNP (classic) | rs245111 |
ClinGen | rs245111 |
ebi | rs245111 |
HLI | rs245111 |
Exac | rs245111 |
Gnomad | rs245111 |
Varsome | rs245111 |
LitVar | rs245111 |
Map | rs245111 |
PheGenI | rs245111 |
Biobank | rs245111 |
1000 genomes | rs245111 |
hgdp | rs245111 |
ensembl | rs245111 |
geneview | rs245111 |
scholar | rs245111 |
rs245111 | |
pharmgkb | rs245111 |
gwascentral | rs245111 |
openSNP | rs245111 |
23andMe | rs245111 |
SNPshot | rs245111 |
SNPdbe | rs245111 |
MSV3d | rs245111 |
GWAS Ctlg | rs245111 |
GMAF | 0.3788 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 19809483] Comparison of human chromosome 19q13 and syntenic region on mouse chromosome 7 reveals absence, in man, of 11.6 Mb containing four mouse calcium-sensing receptor-related sequences: relevance to familial benign hypocalciuric hypercalcaemia type 3