rs1098774
From SNPedia
Merged into | rs261097 |
Orientation | minus |
Stabilized | plus |
Make rs1098774(A;A) |
Make rs1098774(A;C) |
Make rs1098774(C;C) |
Reference | GRCh38 38.1/142 |
Chromosome | 5 |
Position | 102123983 |
is a | snp |
is | mentioned by |
dbSNP | rs1098774 |
dbSNP (classic) | rs1098774 |
ClinGen | rs1098774 |
ebi | rs1098774 |
HLI | rs1098774 |
Exac | rs1098774 |
Gnomad | rs1098774 |
Varsome | rs1098774 |
LitVar | rs1098774 |
Map | rs1098774 |
PheGenI | rs1098774 |
Biobank | rs1098774 |
1000 genomes | rs1098774 |
hgdp | rs1098774 |
ensembl | rs1098774 |
geneview | rs1098774 |
scholar | rs1098774 |
rs1098774 | |
pharmgkb | rs1098774 |
gwascentral | rs1098774 |
openSNP | rs1098774 |
23andMe | rs1098774 |
SNPshot | rs1098774 |
SNPdbe | rs1098774 |
MSV3d | rs1098774 |
GWAS Ctlg | rs1098774 |
Status | Merged into rs261097 |
Max Magnitude | 0 |
[PMID 22018726] Genetic variation in folylpolyglutamate synthase and gamma-glutamyl hydrolase and plasma homocysteine levels in the Singapore Chinese Health Study