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rs7872515

From SNPedia

Orientationplus
Stabilizedplus
Make rs7872515(A;A)
Make rs7872515(A;G)
Make rs7872515(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position92060258
GeneSPTLC1
is asnp
is mentioned by
dbSNPrs7872515
dbSNP (classic)rs7872515
ClinGenrs7872515
ebirs7872515
HLIrs7872515
Exacrs7872515
Gnomadrs7872515
Varsomers7872515
LitVarrs7872515
Maprs7872515
PheGenIrs7872515
Biobankrs7872515
1000 genomesrs7872515
hgdprs7872515
ensemblrs7872515
geneviewrs7872515
scholarrs7872515
googlers7872515
pharmgkbrs7872515
gwascentralrs7872515
openSNPrs7872515
23andMers7872515
SNPshotrs7872515
SNPdbers7872515
MSV3drs7872515
GWAS Ctlgrs7872515
GMAF0.2971
Max Magnitude0
? (A;A) (A;G) (G;G) 28


GWAS snp
PMID [PMID 22688191OA-icon.png]
Trait
Title Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder.
Risk Allele
P-val 6E-7
Odds Ratio 1.3900 None