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rs147815528

From SNPedia

Orientationplus
Stabilizedplus
Make rs147815528(C;C)
Make rs147815528(C;G)
Make rs147815528(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position184795047
GeneFAM129A
is asnp
is mentioned by
dbSNPrs147815528
dbSNP (old)rs147815528
ClinGenrs147815528
ebirs147815528
HLIrs147815528
Exacrs147815528
Varsomers147815528
Maprs147815528
PheGenIrs147815528
Biobankrs147815528
1000 genomesrs147815528
hgdprs147815528
ensemblrs147815528
gopubmedrs147815528
geneviewrs147815528
scholarrs147815528
googlers147815528
pharmgkbrs147815528
gwascentralrs147815528
openSNPrs147815528
23andMers147815528
23andMe allrs147815528
SNP Nexus

SNPshotrs147815528
SNPdbers147815528
MSV3drs147815528
GWAS Ctlgrs147815528
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.