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rs138365897

From SNPedia

Orientationplus
Stabilizedplus
Make rs138365897(C;C)
Make rs138365897(C;T)
Make rs138365897(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position129750474
GeneXPNPEP2
is asnp
is mentioned by
dbSNPrs138365897
dbSNP (old)rs138365897
ClinGenrs138365897
ebirs138365897
HLIrs138365897
Exacrs138365897
Varsomers138365897
Maprs138365897
PheGenIrs138365897
Biobankrs138365897
1000 genomesrs138365897
hgdprs138365897
ensemblrs138365897
gopubmedrs138365897
geneviewrs138365897
scholarrs138365897
googlers138365897
pharmgkbrs138365897
gwascentralrs138365897
openSNPrs138365897
23andMers138365897
23andMe allrs138365897
SNP Nexus

SNPshotrs138365897
SNPdbers138365897
MSV3drs138365897
GWAS Ctlgrs138365897
Max Magnitude
[PMID 27120077] Exome Sequencing of Familial Bipolar Disorder. The minor allele of this SNP is one of 84 rare variants speculated to have an impact (positive or negative; see publication for specific SNP details) on risk for bipolar disorder. The analysis of many more patients is likely to be required to confirm or refute this association.