rs745080
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs745080(C;C) |
Make rs745080(C;T) |
Make rs745080(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 14 |
Position | 52522510 |
Gene | TXNDC16 |
is a | snp |
is | mentioned by |
dbSNP | rs745080 |
dbSNP (classic) | rs745080 |
ClinGen | rs745080 |
ebi | rs745080 |
HLI | rs745080 |
Exac | rs745080 |
Gnomad | rs745080 |
Varsome | rs745080 |
LitVar | rs745080 |
Map | rs745080 |
PheGenI | rs745080 |
Biobank | rs745080 |
1000 genomes | rs745080 |
hgdp | rs745080 |
ensembl | rs745080 |
geneview | rs745080 |
scholar | rs745080 |
rs745080 | |
pharmgkb | rs745080 |
gwascentral | rs745080 |
openSNP | rs745080 |
23andMe | rs745080 |
SNPshot | rs745080 |
SNPdbe | rs745080 |
MSV3d | rs745080 |
GWAS Ctlg | rs745080 |
GMAF | 0.3871 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 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 | 8E-7 |
Odds Ratio | 1.5900 None |
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 14
- Has genotype
- Has population
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip Affy GenomeWide 6
- On chip Ancestry v2
- On chip FTDNA2
- On chip FTDNA
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip NatGeo2
- On chip Ancestry v2c
- On chip Ancestry v2d