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rs1572299

From SNPedia

Orientationminus
Stabilizedminus
Make rs1572299(A;A)
Make rs1572299(A;G)
Make rs1572299(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position118584139
is asnp
is mentioned by
dbSNPrs1572299
ebirs1572299
HLIrs1572299
Exacrs1572299
Varsomers1572299
Maprs1572299
PheGenIrs1572299
hapmaprs1572299
1000 genomesrs1572299
hgdprs1572299
ensemblrs1572299
gopubmedrs1572299
geneviewrs1572299
scholarrs1572299
googlers1572299
pharmgkbrs1572299
gwascentralrs1572299
openSNPrs1572299
23andMers1572299
23andMe allrs1572299
SNP Nexus

SNPshotrs1572299
SNPdbers1572299
MSV3drs1572299
GWAS Ctlgrs1572299
GMAF0.2466
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 19571808OA-icon.png]
Trait Schizophrenia
Title Common variants conferring risk of schizophrenia
Risk Allele A
P-val 0.000004
Odds Ratio 1.08 [NR]


GET Evidence
rs1572299
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.238095
summary