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rs773257111

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 4 hypophosphatasia
(A;G) 3 carrier of a hypophosphatasia allele
(G;G) 0 normal
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position21563143
GeneALPL
is asnp
is mentioned by
dbSNPrs773257111
ebirs773257111
HLIrs773257111
Exacrs773257111
Varsomers773257111
Maprs773257111
PheGenIrs773257111
hapmaprs773257111
1000 genomesrs773257111
hgdprs773257111
ensemblrs773257111
gopubmedrs773257111
geneviewrs773257111
scholarrs773257111
googlers773257111
pharmgkbrs773257111
gwascentralrs773257111
openSNPrs773257111
23andMers773257111
23andMe allrs773257111
SNP Nexus

SNPshotrs773257111
SNPdbers773257111
MSV3drs773257111
GWAS Ctlgrs773257111
Max Magnitude4
rs773257111, also known as c.331G>A or p.A111T, 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.

This SNP is referred to as i6006944 by 23andMe.