rs6601427
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6601427(C;C) |
Make rs6601427(C;T) |
Make rs6601427(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 8 |
Position | 10298515 |
Gene | MSRA |
is a | snp |
is | mentioned by |
dbSNP | rs6601427 |
dbSNP (classic) | rs6601427 |
ClinGen | rs6601427 |
ebi | rs6601427 |
HLI | rs6601427 |
Exac | rs6601427 |
Gnomad | rs6601427 |
Varsome | rs6601427 |
LitVar | rs6601427 |
Map | rs6601427 |
PheGenI | rs6601427 |
Biobank | rs6601427 |
1000 genomes | rs6601427 |
hgdp | rs6601427 |
ensembl | rs6601427 |
geneview | rs6601427 |
scholar | rs6601427 |
rs6601427 | |
pharmgkb | rs6601427 |
gwascentral | rs6601427 |
openSNP | rs6601427 |
23andMe | rs6601427 |
SNPshot | rs6601427 |
SNPdbe | rs6601427 |
MSV3d | rs6601427 |
GWAS Ctlg | rs6601427 |
GMAF | 0.4045 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 22438829] Variation in MSRA Modifies Risk of Neonatal Intestinal Obstruction in Cystic Fibrosis