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rs35555197

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs35555197(A;A)
Make rs35555197(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome6
Position107245583
GenePDSS2
is asnp
is mentioned by
dbSNPrs35555197
ebirs35555197
HLIrs35555197
Exacrs35555197
Varsomers35555197
Maprs35555197
PheGenIrs35555197
hapmaprs35555197
1000 genomesrs35555197
hgdprs35555197
ensemblrs35555197
gopubmedrs35555197
geneviewrs35555197
scholarrs35555197
googlers35555197
pharmgkbrs35555197
gwascentralrs35555197
openSNPrs35555197
23andMers35555197
23andMe allrs35555197
SNP Nexus

SNPshotrs35555197
SNPdbers35555197
MSV3drs35555197
GWAS Ctlgrs35555197
Max Magnitude0
[PMID 27120077] 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.
ClinVar
Risk rs35555197(A;A)
Alt rs35555197(A;A)
Reference rs35555197(G;G)
Significance Unknown
Disease not specified
Variation info
Gene PDSS2
CLNDBN not specified
Reversed 1
HGVS NC_000006.11:g.107566787C>T
CLNSRC
CLNACC RCV000197521.2,