rs121912597
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common on affy axiom data |
Make rs121912597(C;T) |
Make rs121912597(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 143493701 |
Gene | SLC9A9 |
is a | snp |
is | mentioned by |
dbSNP | rs121912597 |
dbSNP (classic) | rs121912597 |
ClinGen | rs121912597 |
ebi | rs121912597 |
HLI | rs121912597 |
Exac | rs121912597 |
Gnomad | rs121912597 |
Varsome | rs121912597 |
LitVar | rs121912597 |
Map | rs121912597 |
PheGenI | rs121912597 |
Biobank | rs121912597 |
1000 genomes | rs121912597 |
hgdp | rs121912597 |
ensembl | rs121912597 |
geneview | rs121912597 |
scholar | rs121912597 |
rs121912597 | |
pharmgkb | rs121912597 |
gwascentral | rs121912597 |
openSNP | rs121912597 |
23andMe | rs121912597 |
SNPshot | rs121912597 |
SNPdbe | rs121912597 |
MSV3d | rs121912597 |
GWAS Ctlg | rs121912597 |
GMAF | 0.0004591 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs121912597(T;T) |
Alt | rs121912597(T;T) |
Reference | Rs121912597(C;C) |
Significance | Other |
Disease | Autism 16 |
Variation | info |
Gene | SLC9A9 |
CLNDBN | Autism 16 |
Reversed | 1 |
HGVS | NC_000003.11:g.143212543G>A |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000002459.3, |