rs797046134
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs797046134(C;C) |
Make rs797046134(C;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 15 |
Position | 100914748 |
Gene | ALDH1A3, LOC101927751 |
is a | snp |
is | mentioned by |
dbSNP | rs797046134 |
dbSNP (classic) | rs797046134 |
ClinGen | rs797046134 |
ebi | rs797046134 |
HLI | rs797046134 |
Exac | rs797046134 |
Gnomad | rs797046134 |
Varsome | rs797046134 |
LitVar | rs797046134 |
Map | rs797046134 |
PheGenI | rs797046134 |
Biobank | rs797046134 |
1000 genomes | rs797046134 |
hgdp | rs797046134 |
ensembl | rs797046134 |
geneview | rs797046134 |
scholar | rs797046134 |
rs797046134 | |
pharmgkb | rs797046134 |
gwascentral | rs797046134 |
openSNP | rs797046134 |
23andMe | rs797046134 |
SNPshot | rs797046134 |
SNPdbe | rs797046134 |
MSV3d | rs797046134 |
GWAS Ctlg | rs797046134 |
Max Magnitude | 0 |
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 | LOC101927751 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, |