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rs368953604

From SNPedia

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Geno Mag Summary
(C;C) 0 common in clinvar
Make rs368953604(C;T)
Make rs368953604(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome9
Position35090061
GenePIGO
is asnp
is mentioned by
dbSNPrs368953604
ebirs368953604
HLIrs368953604
Exacrs368953604
Varsomers368953604
Maprs368953604
PheGenIrs368953604
hapmaprs368953604
1000 genomesrs368953604
hgdprs368953604
ensemblrs368953604
gopubmedrs368953604
geneviewrs368953604
scholarrs368953604
googlers368953604
pharmgkbrs368953604
gwascentralrs368953604
openSNPrs368953604
23andMers368953604
23andMe allrs368953604
SNP Nexus

SNPshotrs368953604
SNPdbers368953604
MSV3drs368953604
GWAS Ctlgrs368953604
Max Magnitude0
ClinVar
Risk rs368953604(T;T)
Alt rs368953604(T;T)
Reference rs368953604(C;C)
Significance Pathogenic
Disease Hyperphosphatasia with mental retardation syndrome 2
Variation info
Gene PIGO
CLNDBN Hyperphosphatasia with mental retardation syndrome 2
Reversed 0
HGVS NC_000009.11:g.35090058C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000029247.3,