Have questions? Visit https://www.reddit.com/r/SNPedia

rs763457259

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
Position21573733
GeneALPL
is asnp
is mentioned by
dbSNPrs763457259
ebirs763457259
HLIrs763457259
Exacrs763457259
Varsomers763457259
Maprs763457259
PheGenIrs763457259
hapmaprs763457259
1000 genomesrs763457259
hgdprs763457259
ensemblrs763457259
gopubmedrs763457259
geneviewrs763457259
scholarrs763457259
googlers763457259
pharmgkbrs763457259
gwascentralrs763457259
openSNPrs763457259
23andMers763457259
23andMe allrs763457259
SNP Nexus

SNPshotrs763457259
SNPdbers763457259
MSV3drs763457259
GWAS Ctlgrs763457259
Max Magnitude4
rs763457259, also known as c.931G>A or p.E311K, 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 perinatal form of hypophosphatasia.

This SNP is referred to as i6006933 by 23andMe.