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rs770591449

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs770591449(-;-)
Make rs770591449(-;G)
Make rs770591449(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome9
Position35091525
GenePIGO
is asnp
is mentioned by
dbSNPrs770591449
ebirs770591449
HLIrs770591449
Exacrs770591449
Varsomers770591449
Maprs770591449
PheGenIrs770591449
hapmaprs770591449
1000 genomesrs770591449
hgdprs770591449
ensemblrs770591449
gopubmedrs770591449
geneviewrs770591449
scholarrs770591449
googlers770591449
pharmgkbrs770591449
gwascentralrs770591449
openSNPrs770591449
23andMers770591449
23andMe allrs770591449
SNP Nexus

SNPshotrs770591449
SNPdbers770591449
MSV3drs770591449
GWAS Ctlgrs770591449
Max Magnitude0
ClinVar
Risk rs770591449(G;G)
Alt rs770591449(G;G)
Reference rs770591449(;)
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.35091523dupG
CLNSRC OMIM Allelic Variant
CLNACC RCV000029246.3,