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rs771540767

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
Position21575879
GeneALPL
is asnp
is mentioned by
dbSNPrs771540767
ebirs771540767
HLIrs771540767
Exacrs771540767
Varsomers771540767
Maprs771540767
PheGenIrs771540767
hapmaprs771540767
1000 genomesrs771540767
hgdprs771540767
ensemblrs771540767
gopubmedrs771540767
geneviewrs771540767
scholarrs771540767
googlers771540767
pharmgkbrs771540767
gwascentralrs771540767
openSNPrs771540767
23andMers771540767
23andMe allrs771540767
SNP Nexus

SNPshotrs771540767
SNPdbers771540767
MSV3drs771540767
GWAS Ctlgrs771540767
Max Magnitude4
rs771540767, also known as c.1144G>A or p.V382I, 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 childhood form of hypophosphatasia.

This SNP is referred to as i6006962 by 23andMe.