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rs773359554

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs773359554(C;T)
Make rs773359554(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position3811305
GenePGAP2
is asnp
is mentioned by
dbSNPrs773359554
ebirs773359554
HLIrs773359554
Exacrs773359554
Varsomers773359554
Maprs773359554
PheGenIrs773359554
hapmaprs773359554
1000 genomesrs773359554
hgdprs773359554
ensemblrs773359554
gopubmedrs773359554
geneviewrs773359554
scholarrs773359554
googlers773359554
pharmgkbrs773359554
gwascentralrs773359554
openSNPrs773359554
23andMers773359554
23andMe allrs773359554
SNP Nexus

SNPshotrs773359554
SNPdbers773359554
MSV3drs773359554
GWAS Ctlgrs773359554
Max Magnitude0
ClinVar
Risk rs773359554(T;T)
Alt rs773359554(T;T)
Reference rs773359554(C;C)
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.3832535C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000043538.2,