rs177216
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in complete genomics |
Make rs177216(A;A) |
Make rs177216(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 14 |
Position | 78063343 |
Gene | NRXN3 |
is a | snp |
is | mentioned by |
dbSNP | rs177216 |
dbSNP (classic) | rs177216 |
ClinGen | rs177216 |
ebi | rs177216 |
HLI | rs177216 |
Exac | rs177216 |
Gnomad | rs177216 |
Varsome | rs177216 |
LitVar | rs177216 |
Map | rs177216 |
PheGenI | rs177216 |
Biobank | rs177216 |
1000 genomes | rs177216 |
hgdp | rs177216 |
ensembl | rs177216 |
geneview | rs177216 |
scholar | rs177216 |
rs177216 | |
pharmgkb | rs177216 |
gwascentral | rs177216 |
openSNP | rs177216 |
23andMe | rs177216 |
SNPshot | rs177216 |
SNPdbe | rs177216 |
MSV3d | rs177216 |
GWAS Ctlg | rs177216 |
GMAF | 0.1056 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 21622161] Confirmation and further mapping of the GLC3C locus in primary congenital glaucoma.