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rs144988758

From SNPedia

Orientationplus
Stabilizedplus
Make rs144988758(C;C)
Make rs144988758(C;T)
Make rs144988758(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position85077454
GeneKIAA0513
is asnp
is mentioned by
dbSNPrs144988758
dbSNP (old)rs144988758
ClinGenrs144988758
ebirs144988758
HLIrs144988758
Exacrs144988758
Gnomadrs144988758
Varsomers144988758
Maprs144988758
PheGenIrs144988758
Biobankrs144988758
1000 genomesrs144988758
hgdprs144988758
ensemblrs144988758
gopubmedrs144988758
geneviewrs144988758
scholarrs144988758
googlers144988758
pharmgkbrs144988758
gwascentralrs144988758
openSNPrs144988758
23andMers144988758
23andMe allrs144988758
SNP Nexus

SNPshotrs144988758
SNPdbers144988758
MSV3drs144988758
GWAS Ctlgrs144988758
Max Magnitude
[PMID 27120077OA-icon.png] 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.