rs150341307
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs150341307(C;C) |
Make rs150341307(C;G) |
Make rs150341307(G;G) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 1 |
Position | 32207913 |
Gene | DCDC2B, IQCC, TMEM234 |
is a | snp |
is | mentioned by |
dbSNP | rs150341307 |
dbSNP (classic) | rs150341307 |
ClinGen | rs150341307 |
ebi | rs150341307 |
HLI | rs150341307 |
Exac | rs150341307 |
Gnomad | rs150341307 |
Varsome | rs150341307 |
LitVar | rs150341307 |
Map | rs150341307 |
PheGenI | rs150341307 |
Biobank | rs150341307 |
1000 genomes | rs150341307 |
hgdp | rs150341307 |
ensembl | rs150341307 |
geneview | rs150341307 |
scholar | rs150341307 |
rs150341307 | |
pharmgkb | rs150341307 |
gwascentral | rs150341307 |
openSNP | rs150341307 |
23andMe | rs150341307 |
SNPshot | rs150341307 |
SNPdbe | rs150341307 |
MSV3d | rs150341307 |
GWAS Ctlg | rs150341307 |
Max Magnitude | 0 |
[PMID 28146470] Rare and low-frequency coding variants alter human adult height.