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rs1502844

From SNPedia

Orientationplus
Stabilizedplus
Make rs1502844(C;C)
Make rs1502844(C;T)
Make rs1502844(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position102523613
is asnp
is mentioned by
dbSNPrs1502844
ebirs1502844
HLIrs1502844
Exacrs1502844
Varsomers1502844
Maprs1502844
PheGenIrs1502844
hapmaprs1502844
1000 genomesrs1502844
hgdprs1502844
ensemblrs1502844
gopubmedrs1502844
geneviewrs1502844
scholarrs1502844
googlers1502844
pharmgkbrs1502844
gwascentralrs1502844
openSNPrs1502844
23andMers1502844
23andMe allrs1502844
SNP Nexus

SNPshotrs1502844
SNPdbers1502844
MSV3drs1502844
GWAS Ctlgrs1502844
GMAF0.3921
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19571808OA-icon.png]
Trait Schizophrenia
Title Common variants conferring risk of schizophrenia
Risk Allele C
P-val 0.000001
Odds Ratio 1.09 [NR]


GET Evidence
rs1502844
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.650794
summary