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rs200257202

From SNPedia

Orientationplus
Stabilizedplus
Make rs200257202(A;A)
Make rs200257202(A;C)
Make rs200257202(C;C)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position55567253
GeneCAPNS2, LPCAT2
is asnp
is mentioned by
dbSNPrs200257202
dbSNP (old)rs200257202
ClinGenrs200257202
ebirs200257202
HLIrs200257202
Exacrs200257202
Varsomers200257202
Maprs200257202
PheGenIrs200257202
Biobankrs200257202
1000 genomesrs200257202
hgdprs200257202
ensemblrs200257202
gopubmedrs200257202
geneviewrs200257202
scholarrs200257202
googlers200257202
pharmgkbrs200257202
gwascentralrs200257202
openSNPrs200257202
23andMers200257202
23andMe allrs200257202
SNP Nexus

SNPshotrs200257202
SNPdbers200257202
MSV3drs200257202
GWAS Ctlgrs200257202
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.