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rs61734270

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs61734270(C;T)
Make rs61734270(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position49524089
GenePTGIS
is asnp
is mentioned by
dbSNPrs61734270
ebirs61734270
HLIrs61734270
Exacrs61734270
Varsomers61734270
Maprs61734270
PheGenIrs61734270
hapmaprs61734270
1000 genomesrs61734270
hgdprs61734270
ensemblrs61734270
gopubmedrs61734270
geneviewrs61734270
scholarrs61734270
googlers61734270
pharmgkbrs61734270
gwascentralrs61734270
openSNPrs61734270
23andMers61734270
23andMe allrs61734270
SNP Nexus

SNPshotrs61734270
SNPdbers61734270
MSV3drs61734270
GWAS Ctlgrs61734270
Max Magnitude0
ClinVar
Risk rs61734270(T;T)
Alt rs61734270(T;T)
Reference rs61734270(C;C)
Significance Probable-Pathogenic
Disease Childhood-Onset Schizophrenia
Variation info
Gene PTGIS
CLNDBN Childhood-Onset Schizophrenia
Reversed 0
HGVS NC_000020.10:g.48140626C>T
CLNSRC
CLNACC RCV000202340.1,