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rs200050453

From SNPedia

Orientationplus
Stabilizedplus
Make rs200050453(A;A)
Make rs200050453(A;C)
Make rs200050453(C;C)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position232464921
GeneSIPA1L2
is asnp
is mentioned by
dbSNPrs200050453
dbSNP (old)rs200050453
ClinGenrs200050453
ebirs200050453
HLIrs200050453
Exacrs200050453
Gnomadrs200050453
Varsomers200050453
Maprs200050453
PheGenIrs200050453
Biobankrs200050453
1000 genomesrs200050453
hgdprs200050453
ensemblrs200050453
gopubmedrs200050453
geneviewrs200050453
scholarrs200050453
googlers200050453
pharmgkbrs200050453
gwascentralrs200050453
openSNPrs200050453
23andMers200050453
23andMe allrs200050453
SNP Nexus

SNPshotrs200050453
SNPdbers200050453
MSV3drs200050453
GWAS Ctlgrs200050453
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.