rs141600901
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs141600901(-;-) |
Make rs141600901(-;AC) |
Make rs141600901(AC;AC) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 15 |
Position | 48739003 |
Gene | CEP152 |
is a | snp |
is | mentioned by |
dbSNP | rs141600901 |
dbSNP (classic) | rs141600901 |
ClinGen | rs141600901 |
ebi | rs141600901 |
HLI | rs141600901 |
Exac | rs141600901 |
Gnomad | rs141600901 |
Varsome | rs141600901 |
LitVar | rs141600901 |
Map | rs141600901 |
PheGenI | rs141600901 |
Biobank | rs141600901 |
1000 genomes | rs141600901 |
hgdp | rs141600901 |
ensembl | rs141600901 |
geneview | rs141600901 |
scholar | rs141600901 |
rs141600901 | |
pharmgkb | rs141600901 |
gwascentral | rs141600901 |
openSNP | rs141600901 |
23andMe | rs141600901 |
SNPshot | rs141600901 |
SNPdbe | rs141600901 |
MSV3d | rs141600901 |
GWAS Ctlg | rs141600901 |
Max Magnitude | 0 |
OMIM pathogenic variant