rs2847324
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2847324(C;C) |
Make rs2847324(C;T) |
Make rs2847324(T;T) |
Reference | GRCh37.p10 37.5/138 |
Chromosome | 18 |
Position | 679637 |
Gene | ENOSF1 |
is a | snp |
is | mentioned by |
dbSNP | rs2847324 |
dbSNP (classic) | rs2847324 |
ClinGen | rs2847324 |
ebi | rs2847324 |
HLI | rs2847324 |
Exac | rs2847324 |
Gnomad | rs2847324 |
Varsome | rs2847324 |
LitVar | rs2847324 |
Map | rs2847324 |
PheGenI | rs2847324 |
Biobank | rs2847324 |
1000 genomes | rs2847324 |
hgdp | rs2847324 |
ensembl | rs2847324 |
geneview | rs2847324 |
scholar | rs2847324 |
rs2847324 | |
pharmgkb | rs2847324 |
gwascentral | rs2847324 |
openSNP | rs2847324 |
23andMe | rs2847324 |
SNPshot | rs2847324 |
SNPdbe | rs2847324 |
MSV3d | rs2847324 |
GWAS Ctlg | rs2847324 |
GMAF | 0.1791 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 24535845] Conotruncal heart defects and common variants in maternal and fetal genes in folate, homocysteine, and transsulfuration pathways