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rs146980221

From SNPedia

Orientationplus
Stabilizedplus
Make rs146980221(A;A)
Make rs146980221(A;G)
Make rs146980221(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position233354955
GeneKIAA1804, MAP3K21
is asnp
is mentioned by
dbSNPrs146980221
dbSNP (old)rs146980221
ClinGenrs146980221
ebirs146980221
HLIrs146980221
Exacrs146980221
Gnomadrs146980221
Varsomers146980221
Maprs146980221
PheGenIrs146980221
Biobankrs146980221
1000 genomesrs146980221
hgdprs146980221
ensemblrs146980221
gopubmedrs146980221
geneviewrs146980221
scholarrs146980221
googlers146980221
pharmgkbrs146980221
gwascentralrs146980221
openSNPrs146980221
23andMers146980221
23andMe allrs146980221
SNP Nexus

SNPshotrs146980221
SNPdbers146980221
MSV3drs146980221
GWAS Ctlgrs146980221
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.