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rs1443548

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1443548(C;C)
Make rs1443548(C;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position20601496
GeneSLC6A5
is asnp
is mentioned by
dbSNPrs1443548
dbSNP (classic)rs1443548
ClinGenrs1443548
ebirs1443548
HLIrs1443548
Exacrs1443548
Gnomadrs1443548
Varsomers1443548
LitVarrs1443548
Maprs1443548
PheGenIrs1443548
Biobankrs1443548
1000 genomesrs1443548
hgdprs1443548
ensemblrs1443548
geneviewrs1443548
scholarrs1443548
googlers1443548
pharmgkbrs1443548
gwascentralrs1443548
openSNPrs1443548
23andMers1443548
SNPshotrs1443548
SNPdbers1443548
MSV3drs1443548
GWAS Ctlgrs1443548
GMAF0.2107
Max Magnitude0
? (C;C) (C;T) (T;T) 28


[PMID 20859245] Glutamatergic gene variants impact the clinical profile of efficacy and side effects of haloperidol



ClinVar
Risk rs1443548(C;C)
Alt rs1443548(C;C)
Reference Rs1443548(T;T)
Significance Non-pathogenic
Disease Hyperekplexia
Variation info
Gene SLC6A5
CLNDBN Hyperekplexia
Reversed 0
HGVS NC_000011.9:g.20623042T>C
CLNSRC
CLNACC RCV000365666.1,