rs3832406
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common/normal |
Make rs3832406(-;ATT) |
Make rs3832406(ATT;ATT) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 150898848 |
Gene | MTHFD1L |
is a | snp |
is | mentioned by |
dbSNP | rs3832406 |
dbSNP (classic) | rs3832406 |
ClinGen | rs3832406 |
ebi | rs3832406 |
HLI | rs3832406 |
Exac | rs3832406 |
Gnomad | rs3832406 |
Varsome | rs3832406 |
LitVar | rs3832406 |
Map | rs3832406 |
PheGenI | rs3832406 |
Biobank | rs3832406 |
1000 genomes | rs3832406 |
hgdp | rs3832406 |
ensembl | rs3832406 |
geneview | rs3832406 |
scholar | rs3832406 |
rs3832406 | |
pharmgkb | rs3832406 |
gwascentral | rs3832406 |
openSNP | rs3832406 |
23andMe | rs3832406 |
SNPshot | rs3832406 |
SNPdbe | rs3832406 |
MSV3d | rs3832406 |
GWAS Ctlg | rs3832406 |
Max Magnitude | 0 |
[PMID 19777576] A common variant in MTHFD1L is associated with neural tube defects and mRNA splicing efficiency