rs2747022
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2747022(C;C) |
Make rs2747022(C;T) |
Make rs2747022(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | X |
Position | 132126844 |
Gene | FRMD7 |
is a | snp |
is | mentioned by |
dbSNP | rs2747022 |
dbSNP (classic) | rs2747022 |
ClinGen | rs2747022 |
ebi | rs2747022 |
HLI | rs2747022 |
Exac | rs2747022 |
Gnomad | rs2747022 |
Varsome | rs2747022 |
LitVar | rs2747022 |
Map | rs2747022 |
PheGenI | rs2747022 |
Biobank | rs2747022 |
1000 genomes | rs2747022 |
hgdp | rs2747022 |
ensembl | rs2747022 |
geneview | rs2747022 |
scholar | rs2747022 |
rs2747022 | |
pharmgkb | rs2747022 |
gwascentral | rs2747022 |
openSNP | rs2747022 |
23andMe | rs2747022 |
SNPshot | rs2747022 |
SNPdbe | rs2747022 |
MSV3d | rs2747022 |
GWAS Ctlg | rs2747022 |
GMAF | 0.3513 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 23613933] X-Chromosomal Maternal and Fetal SNPs and the Risk of Spontaneous Preterm Delivery in a Danish/Norwegian Genome-Wide Association Study