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rs8150

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs8150(C;G)
Make rs8150(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position76470935
GeneAANAT, RHBDF2
is asnp
is mentioned by
dbSNPrs8150
dbSNP (classic)rs8150
ClinGenrs8150
ebirs8150
HLIrs8150
Exacrs8150
Gnomadrs8150
Varsomers8150
LitVarrs8150
Maprs8150
PheGenIrs8150
Biobankrs8150
1000 genomesrs8150
hgdprs8150
ensemblrs8150
geneviewrs8150
scholarrs8150
googlers8150
pharmgkbrs8150
gwascentralrs8150
openSNPrs8150
23andMers8150
SNPshotrs8150
SNPdbers8150
MSV3drs8150
GWAS Ctlgrs8150
GMAF0.3898
Max Magnitude0
? (C;C) (C;G) (G;G) 28


[PMID 20459461] Resequencing and association analysis of arylalkylamine N-acetyltransferase (AANAT) gene and its contribution to major depression susceptibility


[PMID 19184136OA-icon.png] Examination of association of genes in the serotonin system to autism.


[PMID 25229211] Polymorphisms in circadian genes, night work and breast cancer: results from the GENICA study


ClinVar
Risk rs8150(G;G) rs8150(T;T)
Alt rs8150(G;G) rs8150(T;T)
Reference Rs8150(C;C)
Significance Non-pathogenic
Disease Howel-Evans syndrome
Variation info
Gene RHBDF2
CLNDBN Howel-Evans syndrome
Reversed 1
HGVS NC_000017.10:g.74467017G>C
CLNSRC
CLNACC RCV000284468.1,