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rs797046134

From SNPedia

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Geno Mag Summary
(T;T) 0 common in clinvar
Make rs797046134(C;C)
Make rs797046134(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position100914748
GeneALDH1A3
is asnp
is mentioned by
dbSNPrs797046134
ebirs797046134
HLIrs797046134
Exacrs797046134
Varsomers797046134
Maprs797046134
PheGenIrs797046134
hapmaprs797046134
1000 genomesrs797046134
hgdprs797046134
ensemblrs797046134
gopubmedrs797046134
geneviewrs797046134
scholarrs797046134
googlers797046134
pharmgkbrs797046134
gwascentralrs797046134
openSNPrs797046134
23andMers797046134
23andMe allrs797046134
SNP Nexus

SNPshotrs797046134
SNPdbers797046134
MSV3drs797046134
GWAS Ctlgrs797046134
Max Magnitude0
ClinVar
Risk rs797046134(C;C)
Alt rs797046134(C;C)
Reference rs797046134(T;T)
Significance Probable-Pathogenic
Disease Autistic disorder of childhood onset
Variation info
Gene ALDH1A3
CLNDBN Autistic disorder of childhood onset
Reversed 0
HGVS NC_000015.9:g.101454953T>C
CLNSRC Laboratorio de Genetica Humana\x3bUniversidad de los Andes
CLNACC RCV000194309.1,