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

rs371058193

From SNPedia

Orientationplus
Stabilizedplus
Make rs371058193(C;C)
Make rs371058193(C;G)
Make rs371058193(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position20037468
GeneCRNKL1
is asnp
is mentioned by
dbSNPrs371058193
dbSNP (old)rs371058193
ClinGenrs371058193
ebirs371058193
HLIrs371058193
Exacrs371058193
Gnomadrs371058193
Varsomers371058193
Maprs371058193
PheGenIrs371058193
Biobankrs371058193
1000 genomesrs371058193
hgdprs371058193
ensemblrs371058193
gopubmedrs371058193
geneviewrs371058193
scholarrs371058193
googlers371058193
pharmgkbrs371058193
gwascentralrs371058193
openSNPrs371058193
23andMers371058193
23andMe allrs371058193
SNP Nexus

SNPshotrs371058193
SNPdbers371058193
MSV3drs371058193
GWAS Ctlgrs371058193
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.