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rs869025322

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs869025322(C;C)
Make rs869025322(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome4
Position88521653
GenePIGY, PYURF
is asnp
is mentioned by
dbSNPrs869025322
ebirs869025322
HLIrs869025322
Exacrs869025322
Varsomers869025322
Maprs869025322
PheGenIrs869025322
hapmaprs869025322
1000 genomesrs869025322
hgdprs869025322
ensemblrs869025322
gopubmedrs869025322
geneviewrs869025322
scholarrs869025322
googlers869025322
pharmgkbrs869025322
gwascentralrs869025322
openSNPrs869025322
23andMers869025322
23andMe allrs869025322
SNP Nexus

SNPshotrs869025322
SNPdbers869025322
MSV3drs869025322
GWAS Ctlgrs869025322
Max Magnitude0
ClinVar
Risk rs869025322(C;C)
Alt rs869025322(C;C)
Reference rs869025322(T;T)
Significance Pathogenic
Disease Hyperphosphatasia with mental retardation syndrome 6
Variation info
Gene PIGY PYURF
CLNDBN Hyperphosphatasia with mental retardation syndrome 6
Reversed 1
HGVS NC_000004.11:g.89442804A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000207478.1,