rs41286560
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs41286560(G;G) |
Make rs41286560(G;T) |
Make rs41286560(T;T) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 14 |
Position | 100883117 |
Gene | MIR127, MIR136, MIR432, RTL1 |
is a | snp |
is | mentioned by |
dbSNP | rs41286560 |
dbSNP (classic) | rs41286560 |
ClinGen | rs41286560 |
ebi | rs41286560 |
HLI | rs41286560 |
Exac | rs41286560 |
Gnomad | rs41286560 |
Varsome | rs41286560 |
LitVar | rs41286560 |
Map | rs41286560 |
PheGenI | rs41286560 |
Biobank | rs41286560 |
1000 genomes | rs41286560 |
hgdp | rs41286560 |
ensembl | rs41286560 |
geneview | rs41286560 |
scholar | rs41286560 |
rs41286560 | |
pharmgkb | rs41286560 |
gwascentral | rs41286560 |
openSNP | rs41286560 |
23andMe | rs41286560 |
SNPshot | rs41286560 |
SNPdbe | rs41286560 |
MSV3d | rs41286560 |
GWAS Ctlg | rs41286560 |
Max Magnitude | 0 |
[PMID 28146470] Rare and low-frequency coding variants alter human adult height.