rs1208285
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1208285(C;C) |
Make rs1208285(C;T) |
Make rs1208285(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 133837662 |
Gene | LINC01312, TARID |
is a | snp |
is | mentioned by |
dbSNP | rs1208285 |
dbSNP (classic) | rs1208285 |
ClinGen | rs1208285 |
ebi | rs1208285 |
HLI | rs1208285 |
Exac | rs1208285 |
Gnomad | rs1208285 |
Varsome | rs1208285 |
LitVar | rs1208285 |
Map | rs1208285 |
PheGenI | rs1208285 |
Biobank | rs1208285 |
1000 genomes | rs1208285 |
hgdp | rs1208285 |
ensembl | rs1208285 |
geneview | rs1208285 |
scholar | rs1208285 |
rs1208285 | |
pharmgkb | rs1208285 |
gwascentral | rs1208285 |
openSNP | rs1208285 |
23andMe | rs1208285 |
SNPshot | rs1208285 |
SNPdbe | rs1208285 |
MSV3d | rs1208285 |
GWAS Ctlg | rs1208285 |
GMAF | 0.2842 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 22306654] |
Trait | |
Title | Common variants near MBNL1 and NKX2-5 are associated with infantile hypertrophic pyloric stenosis. |
Risk Allele | C |
P-val | 6E-7 |
Odds Ratio | 1.2500 None |