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rs879255232

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs879255232(A;G)
Make rs879255232(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position3824013
GenePGAP2
is asnp
is mentioned by
dbSNPrs879255232
ebirs879255232
HLIrs879255232
Exacrs879255232
Varsomers879255232
Maprs879255232
PheGenIrs879255232
hapmaprs879255232
1000 genomesrs879255232
hgdprs879255232
ensemblrs879255232
gopubmedrs879255232
geneviewrs879255232
scholarrs879255232
googlers879255232
pharmgkbrs879255232
gwascentralrs879255232
openSNPrs879255232
23andMers879255232
23andMe allrs879255232
SNP Nexus

SNPshotrs879255232
SNPdbers879255232
MSV3drs879255232
GWAS Ctlgrs879255232
Max Magnitude0
ClinVar
Risk rs879255232(G;G)
Alt rs879255232(G;G)
Reference rs879255232(A;A)
Significance Pathogenic
Disease Hyperphosphatasia with mental retardation syndrome 3
Variation info
Gene PGAP2
CLNDBN Hyperphosphatasia with mental retardation syndrome 3
Reversed 0
HGVS NC_000011.9:g.3845243A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000043535.3,