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

rs142554860

From SNPedia

Orientationplus
Stabilizedplus
Make rs142554860(A;A)
Make rs142554860(A;G)
Make rs142554860(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome10
Position21730926
GeneLOC107984214, MLLT10
is asnp
is mentioned by
dbSNPrs142554860
dbSNP (old)rs142554860
ClinGenrs142554860
ebirs142554860
HLIrs142554860
Exacrs142554860
Gnomadrs142554860
Varsomers142554860
Maprs142554860
PheGenIrs142554860
Biobankrs142554860
1000 genomesrs142554860
hgdprs142554860
ensemblrs142554860
gopubmedrs142554860
geneviewrs142554860
scholarrs142554860
googlers142554860
pharmgkbrs142554860
gwascentralrs142554860
openSNPrs142554860
23andMers142554860
23andMe allrs142554860
SNP Nexus

SNPshotrs142554860
SNPdbers142554860
MSV3drs142554860
GWAS Ctlgrs142554860
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.