rs6799734
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6799734(C;C) |
Make rs6799734(C;G) |
Make rs6799734(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 25444320 |
Gene | RARB |
is a | snp |
is | mentioned by |
dbSNP | rs6799734 |
dbSNP (classic) | rs6799734 |
ClinGen | rs6799734 |
ebi | rs6799734 |
HLI | rs6799734 |
Exac | rs6799734 |
Gnomad | rs6799734 |
Varsome | rs6799734 |
LitVar | rs6799734 |
Map | rs6799734 |
PheGenI | rs6799734 |
Biobank | rs6799734 |
1000 genomes | rs6799734 |
hgdp | rs6799734 |
ensembl | rs6799734 |
geneview | rs6799734 |
scholar | rs6799734 |
rs6799734 | |
pharmgkb | rs6799734 |
gwascentral | rs6799734 |
openSNP | rs6799734 |
23andMe | rs6799734 |
SNPshot | rs6799734 |
SNPdbe | rs6799734 |
MSV3d | rs6799734 |
GWAS Ctlg | rs6799734 |
GMAF | 0.4789 |
Max Magnitude | 0 |
? | (C;C) (C;G) (G;G) | 28 |
---|---|---|
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[PMID 21125561] Association of retinoic acid receptor genes with meningomyelocele [PMID 21254357] Association of retinoic acid receptor genes with meningomyelocele.