Have questions? Visit https://www.reddit.com/r/SNPedia

rs587776934

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587776934(A;A)
Make rs587776934(A;G)
ReferenceGRCh38 38.1/142
Chromosome19
Position18162974
GenePIK3R2
is asnp
is mentioned by
dbSNPrs587776934
ebirs587776934
HLIrs587776934
Exacrs587776934
Varsomers587776934
Maprs587776934
PheGenIrs587776934
hapmaprs587776934
1000 genomesrs587776934
hgdprs587776934
ensemblrs587776934
gopubmedrs587776934
geneviewrs587776934
scholarrs587776934
googlers587776934
pharmgkbrs587776934
gwascentralrs587776934
openSNPrs587776934
23andMers587776934
23andMe allrs587776934
SNP Nexus

SNPshotrs587776934
SNPdbers587776934
MSV3drs587776934
GWAS Ctlgrs587776934
Max Magnitude0
ClinVar
Risk rs587776934(A;A)
Alt rs587776934(A;A)
Reference rs587776934(G;G)
Significance Other
Disease Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 1 Inborn genetic diseases
Variation info
Gene PIK3R2
CLNDBN Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 1 Inborn genetic diseases
Reversed 0
HGVS NC_000019.9:g.18273784G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000033029.4, RCV000190661.1,