Have questions? Visit https://www.reddit.com/r/SNPedia

rs13107595

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs13107595(A;G)
Make rs13107595(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position94657437
GenePDLIM5
is asnp
is mentioned by
dbSNPrs13107595
ebirs13107595
HLIrs13107595
Exacrs13107595
Varsomers13107595
Maprs13107595
PheGenIrs13107595
hapmaprs13107595
1000 genomesrs13107595
hgdprs13107595
ensemblrs13107595
gopubmedrs13107595
geneviewrs13107595
scholarrs13107595
googlers13107595
pharmgkbrs13107595
gwascentralrs13107595
openSNPrs13107595
23andMers13107595
23andMe allrs13107595
SNP Nexus

SNPshotrs13107595
SNPdbers13107595
MSV3drs13107595
GWAS Ctlgrs13107595
GMAF0.01056
Max Magnitude0
? (A;A) (A;G) (G;G) 28
Venter snp
Source plos
Gene PDLIM5
allele A
frequency 0.992
sift TOLERATED
HuRef 1103654486841
Disease Association May play a role in genetic susceptibility to schizophrenia. PDLIM5 is commonly increased in the brain of patients with bipolar disorder, schizophrenia, and major depression.



GET Evidence
PDLIM5-S492N
aa_change Ser492Asn
aa_change_short S492N
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.983547
summary