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rs16897515

From SNPedia

Orientationplus
Stabilizedplus
Make rs16897515(A;A)
Make rs16897515(A;C)
Make rs16897515(C;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position27310241
GenePOM121L2
is asnp
is mentioned by
dbSNPrs16897515
ebirs16897515
HLIrs16897515
Exacrs16897515
Varsomers16897515
Maprs16897515
PheGenIrs16897515
hapmaprs16897515
1000 genomesrs16897515
hgdprs16897515
ensemblrs16897515
gopubmedrs16897515
geneviewrs16897515
scholarrs16897515
googlers16897515
pharmgkbrs16897515
gwascentralrs16897515
openSNPrs16897515
23andMers16897515
23andMe allrs16897515
SNP Nexus

SNPshotrs16897515
SNPdbers16897515
MSV3drs16897515
GWAS Ctlgrs16897515
GMAF0.146
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 23571483]
Trait Schizophrenia
Title A comprehensive family-based replication study of schizophrenia genes.
Risk Allele C
P-val 4E-7
Odds Ratio 1.30 [NR]
GWAS snp
PMID [PMID 23894747]
Trait Schizophrenia
Title A comprehensive family-based replication study of schizophrenia genes.
Risk Allele C
P-val 4E-7
Odds Ratio 1.30 [NR]


[PMID 19571809OA-icon.png] Common variants on chromosome 6p22.1 are associated with schizophrenia.