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rs3816995

From SNPedia

Orientationplus
Stabilizedplus
Make rs3816995(A;A)
Make rs3816995(A;G)
Make rs3816995(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position73339121
GeneSDK2
is asnp
is mentioned by
dbSNPrs3816995
ebirs3816995
HLIrs3816995
Exacrs3816995
Varsomers3816995
Maprs3816995
PheGenIrs3816995
hapmaprs3816995
1000 genomesrs3816995
hgdprs3816995
ensemblrs3816995
gopubmedrs3816995
geneviewrs3816995
scholarrs3816995
googlers3816995
pharmgkbrs3816995
gwascentralrs3816995
openSNPrs3816995
23andMers3816995
23andMe allrs3816995
SNP Nexus

SNPshotrs3816995
SNPdbers3816995
MSV3drs3816995
GWAS Ctlgrs3816995
GMAF0.3471
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 19165232]
Trait Panic disorder
Title Genome-wide association study of panic disorder in the Japanese population
Risk Allele
P-val 2E-7
Odds Ratio NR NR



GET Evidence
rs3816995
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.32
summary