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rs772432010

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 normal
(A;G) 3 carrier of a hypophosphatasia allele
(G;G) 4 hypophosphatasia
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position21568110
GeneALPL
is asnp
is mentioned by
dbSNPrs772432010
ebirs772432010
HLIrs772432010
Exacrs772432010
Varsomers772432010
Maprs772432010
PheGenIrs772432010
hapmaprs772432010
1000 genomesrs772432010
hgdprs772432010
ensemblrs772432010
gopubmedrs772432010
geneviewrs772432010
scholarrs772432010
googlers772432010
pharmgkbrs772432010
gwascentralrs772432010
openSNPrs772432010
23andMers772432010
23andMe allrs772432010
SNP Nexus

SNPshotrs772432010
SNPdbers772432010
MSV3drs772432010
GWAS Ctlgrs772432010
Max Magnitude4
rs772432010, also known as c.655A>G or p.M219V, 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 odonto form of hypophosphatasia.