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rs200992316

From SNPedia

Orientationplus
Stabilizedplus
Make rs200992316(A;A)
Make rs200992316(A;G)
Make rs200992316(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome7
Position5377539
GeneTNRC18
is asnp
is mentioned by
dbSNPrs200992316
dbSNP (old)rs200992316
ClinGenrs200992316
ebirs200992316
HLIrs200992316
Exacrs200992316
Gnomadrs200992316
Varsomers200992316
Maprs200992316
PheGenIrs200992316
Biobankrs200992316
1000 genomesrs200992316
hgdprs200992316
ensemblrs200992316
gopubmedrs200992316
geneviewrs200992316
scholarrs200992316
googlers200992316
pharmgkbrs200992316
gwascentralrs200992316
openSNPrs200992316
23andMers200992316
23andMe allrs200992316
SNP Nexus

SNPshotrs200992316
SNPdbers200992316
MSV3drs200992316
GWAS Ctlgrs200992316
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.