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rs863225094

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863225094(A;A)
Make rs863225094(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position52213076
GenePPP2R1A
is asnp
is mentioned by
dbSNPrs863225094
ebirs863225094
HLIrs863225094
Exacrs863225094
Varsomers863225094
Maprs863225094
PheGenIrs863225094
hapmaprs863225094
1000 genomesrs863225094
hgdprs863225094
ensemblrs863225094
gopubmedrs863225094
geneviewrs863225094
scholarrs863225094
googlers863225094
pharmgkbrs863225094
gwascentralrs863225094
openSNPrs863225094
23andMers863225094
23andMe allrs863225094
SNP Nexus

SNPshotrs863225094
SNPdbers863225094
MSV3drs863225094
GWAS Ctlgrs863225094
Max Magnitude0
ClinVar
Risk rs863225094(A;A)
Alt rs863225094(A;A)
Reference rs863225094(G;G)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene PPP2R1A
CLNDBN Mental retardation, autosomal dominant 36
Reversed 0
HGVS NC_000019.9:g.52716329G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000201504.1,