rs199669988
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 4 | hypophosphatasia |
(A;G) | 3 | carrier of a hypophosphatasia allele |
(G;G) | 0 | normal |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 1 |
Position | 21564097 |
Gene | ALPL |
is a | snp |
is | mentioned by |
dbSNP | rs199669988 |
dbSNP (classic) | rs199669988 |
ClinGen | rs199669988 |
ebi | rs199669988 |
HLI | rs199669988 |
Exac | rs199669988 |
Gnomad | rs199669988 |
Varsome | rs199669988 |
LitVar | rs199669988 |
Map | rs199669988 |
PheGenI | rs199669988 |
Biobank | rs199669988 |
1000 genomes | rs199669988 |
hgdp | rs199669988 |
ensembl | rs199669988 |
geneview | rs199669988 |
scholar | rs199669988 |
rs199669988 | |
pharmgkb | rs199669988 |
gwascentral | rs199669988 |
openSNP | rs199669988 |
23andMe | rs199669988 |
SNPshot | rs199669988 |
SNPdbe | rs199669988 |
MSV3d | rs199669988 |
GWAS Ctlg | rs199669988 |
Max Magnitude | 4 |
rs199669988, also known as c.529G>A or p.A177T, is a SNP in the ALPL gene on chromosome 1.
Based on the ALPL gene mutations database, the rare/minor allele is considered pathogenic for the adult form of hypophosphatasia.
This SNP is referred to as i6006948 by 23andMe.