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

rs745452577

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs745452577(A;A)
Make rs745452577(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position21865798
GeneHSPG2
is asnp
is mentioned by
dbSNPrs745452577
ebirs745452577
HLIrs745452577
Exacrs745452577
Varsomers745452577
Maprs745452577
PheGenIrs745452577
hapmaprs745452577
1000 genomesrs745452577
hgdprs745452577
ensemblrs745452577
gopubmedrs745452577
geneviewrs745452577
scholarrs745452577
googlers745452577
pharmgkbrs745452577
gwascentralrs745452577
openSNPrs745452577
23andMers745452577
23andMe allrs745452577
SNP Nexus

SNPshotrs745452577
SNPdbers745452577
MSV3drs745452577
GWAS Ctlgrs745452577
Max Magnitude0
ClinVar
Risk rs745452577(A;A)
Alt rs745452577(A;A)
Reference rs745452577(G;G)
Significance Probable-Pathogenic
Disease Childhood-Onset Schizophrenia
Variation info
Gene HSPG2
CLNDBN Childhood-Onset Schizophrenia
Reversed 0
HGVS NC_000001.10:g.22192291G>A
CLNSRC
CLNACC RCV000202344.1,