rs267606567
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(I;I) | 0 | common genotype |
Make rs267606567(-;-) |
Make rs267606567(-;AGGAGA) |
Make rs267606567(AGGAGA;AGGAGA) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 11 |
Position | 67483224 |
Gene | AIP |
is a | snp |
is | mentioned by |
dbSNP | rs267606567 |
dbSNP (classic) | rs267606567 |
ClinGen | rs267606567 |
ebi | rs267606567 |
HLI | rs267606567 |
Exac | rs267606567 |
Gnomad | rs267606567 |
Varsome | rs267606567 |
LitVar | rs267606567 |
Map | rs267606567 |
PheGenI | rs267606567 |
Biobank | rs267606567 |
1000 genomes | rs267606567 |
hgdp | rs267606567 |
ensembl | rs267606567 |
geneview | rs267606567 |
scholar | rs267606567 |
rs267606567 | |
pharmgkb | rs267606567 |
gwascentral | rs267606567 |
openSNP | rs267606567 |
23andMe | rs267606567 |
SNPshot | rs267606567 |
SNPdbe | rs267606567 |
MSV3d | rs267606567 |
GWAS Ctlg | rs267606567 |
Max Magnitude | 0 |
OMIM pathogenic variant