rs1328369
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs1328369(A;A) |
Make rs1328369(A;G) |
Make rs1328369(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 13 |
Position | 93260737 |
Gene | GPC6 |
is a | snp |
is | mentioned by |
dbSNP | rs1328369 |
dbSNP (classic) | rs1328369 |
ClinGen | rs1328369 |
ebi | rs1328369 |
HLI | rs1328369 |
Exac | rs1328369 |
Gnomad | rs1328369 |
Varsome | rs1328369 |
LitVar | rs1328369 |
Map | rs1328369 |
PheGenI | rs1328369 |
Biobank | rs1328369 |
1000 genomes | rs1328369 |
hgdp | rs1328369 |
ensembl | rs1328369 |
geneview | rs1328369 |
scholar | rs1328369 |
rs1328369 | |
pharmgkb | rs1328369 |
gwascentral | rs1328369 |
openSNP | rs1328369 |
23andMe | rs1328369 |
SNPshot | rs1328369 |
SNPdbe | rs1328369 |
MSV3d | rs1328369 |
GWAS Ctlg | rs1328369 |
GMAF | 0.376 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 19061984] PTHR1 loss-of-function mutations in familial, nonsyndromic primary failure of tooth eruption.