rs1136747
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1136747(C;C) |
Make rs1136747(C;T) |
Make rs1136747(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 18269327 |
Gene | SAA1 |
is a | snp |
is | mentioned by |
dbSNP | rs1136747 |
dbSNP (classic) | rs1136747 |
ClinGen | rs1136747 |
ebi | rs1136747 |
HLI | rs1136747 |
Exac | rs1136747 |
Gnomad | rs1136747 |
Varsome | rs1136747 |
LitVar | rs1136747 |
Map | rs1136747 |
PheGenI | rs1136747 |
Biobank | rs1136747 |
1000 genomes | rs1136747 |
hgdp | rs1136747 |
ensembl | rs1136747 |
geneview | rs1136747 |
scholar | rs1136747 |
rs1136747 | |
pharmgkb | rs1136747 |
gwascentral | rs1136747 |
openSNP | rs1136747 |
23andMe | rs1136747 |
SNPshot | rs1136747 |
SNPdbe | rs1136747 |
MSV3d | rs1136747 |
GWAS Ctlg | rs1136747 |
GMAF | 0.4086 |
Max Magnitude | 0 |
[PMID 18389087] Rarity of Somatic Mutation and Frequency of Normal Sequence Variation Detected in Sporadic Colon Adenocarcinoma Using High-Throughput cDNA Sequencing.