rs1459579613
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common/normal |
Make rs1459579613(A;A) |
Make rs1459579613(A;G) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 17 |
Position | 80210868 |
Gene | SGSH |
is a | snp |
is | mentioned by |
dbSNP | rs1459579613 |
dbSNP (classic) | rs1459579613 |
ClinGen | rs1459579613 |
ebi | rs1459579613 |
HLI | rs1459579613 |
Exac | rs1459579613 |
Gnomad | rs1459579613 |
Varsome | rs1459579613 |
LitVar | rs1459579613 |
Map | rs1459579613 |
PheGenI | rs1459579613 |
Biobank | rs1459579613 |
1000 genomes | rs1459579613 |
hgdp | rs1459579613 |
ensembl | rs1459579613 |
geneview | rs1459579613 |
scholar | rs1459579613 |
rs1459579613 | |
pharmgkb | rs1459579613 |
gwascentral | rs1459579613 |
openSNP | rs1459579613 |
23andMe | rs1459579613 |
SNPshot | rs1459579613 |
SNPdbe | rs1459579613 |
MSV3d | rs1459579613 |
GWAS Ctlg | rs1459579613 |
Max Magnitude | 0 |
aka c.1093C>T