rs4703822
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs4703822(A;A) |
Make rs4703822(A;G) |
Make rs4703822(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 81115402 |
Gene | RASGRF2 |
is a | snp |
is | mentioned by |
dbSNP | rs4703822 |
dbSNP (classic) | rs4703822 |
ClinGen | rs4703822 |
ebi | rs4703822 |
HLI | rs4703822 |
Exac | rs4703822 |
Gnomad | rs4703822 |
Varsome | rs4703822 |
LitVar | rs4703822 |
Map | rs4703822 |
PheGenI | rs4703822 |
Biobank | rs4703822 |
1000 genomes | rs4703822 |
hgdp | rs4703822 |
ensembl | rs4703822 |
geneview | rs4703822 |
scholar | rs4703822 |
rs4703822 | |
pharmgkb | rs4703822 |
gwascentral | rs4703822 |
openSNP | rs4703822 |
23andMe | rs4703822 |
SNPshot | rs4703822 |
SNPdbe | rs4703822 |
MSV3d | rs4703822 |
GWAS Ctlg | rs4703822 |
GMAF | 0.2635 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 22419666] |
Trait | |
Title | Genome wide study of maternal and parent-of-origin effects on the etiology of orofacial clefts. |
Risk Allele | |
P-val | 0.000004 |
Odds Ratio | 1.5900 None |
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 5
- Has genotype
- Has population
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip Ancestry v2
- On chip FTDNA2
- On chip FTDNA
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip NatGeo2
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d