rs140853839
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs140853839(C;T) |
Make rs140853839(T;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 12 |
Position | 120738874 |
Gene | ACADS |
is a | snp |
is | mentioned by |
dbSNP | rs140853839 |
dbSNP (classic) | rs140853839 |
ClinGen | rs140853839 |
ebi | rs140853839 |
HLI | rs140853839 |
Exac | rs140853839 |
Gnomad | rs140853839 |
Varsome | rs140853839 |
LitVar | rs140853839 |
Map | rs140853839 |
PheGenI | rs140853839 |
Biobank | rs140853839 |
1000 genomes | rs140853839 |
hgdp | rs140853839 |
ensembl | rs140853839 |
geneview | rs140853839 |
scholar | rs140853839 |
rs140853839 | |
pharmgkb | rs140853839 |
gwascentral | rs140853839 |
openSNP | rs140853839 |
23andMe | rs140853839 |
SNPshot | rs140853839 |
SNPdbe | rs140853839 |
MSV3d | rs140853839 |
GWAS Ctlg | rs140853839 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs140853839(A;A) rs140853839(T;T) |
Alt | rs140853839(A;A) rs140853839(T;T) |
Reference | Rs140853839(C;C) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | ACADS |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000012.11:g.121176677C>T |
CLNSRC | |
CLNACC | RCV000185690.2, |