rs781065280
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs781065280(A;A) |
Make rs781065280(A;G) |
Make rs781065280(G;G) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 14 |
Position | 64419926 |
Gene | MTHFD1 |
is a | snp |
is | mentioned by |
dbSNP | rs781065280 |
dbSNP (classic) | rs781065280 |
ClinGen | rs781065280 |
ebi | rs781065280 |
HLI | rs781065280 |
Exac | rs781065280 |
Gnomad | rs781065280 |
Varsome | rs781065280 |
LitVar | rs781065280 |
Map | rs781065280 |
PheGenI | rs781065280 |
Biobank | rs781065280 |
1000 genomes | rs781065280 |
hgdp | rs781065280 |
ensembl | rs781065280 |
geneview | rs781065280 |
scholar | rs781065280 |
rs781065280 | |
pharmgkb | rs781065280 |
gwascentral | rs781065280 |
openSNP | rs781065280 |
23andMe | rs781065280 |
SNPshot | rs781065280 |
SNPdbe | rs781065280 |
MSV3d | rs781065280 |
GWAS Ctlg | rs781065280 |
Max Magnitude | 0 |
aka NM_005956.3(MTHFD1):c.727+1G>A
OMIM pathogenic variant