rs201954387
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs201954387(A;A) |
Make rs201954387(A;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 16 |
Position | 89146044 |
Gene | ACSF3 |
is a | snp |
is | mentioned by |
dbSNP | rs201954387 |
dbSNP (classic) | rs201954387 |
ClinGen | rs201954387 |
ebi | rs201954387 |
HLI | rs201954387 |
Exac | rs201954387 |
Gnomad | rs201954387 |
Varsome | rs201954387 |
LitVar | rs201954387 |
Map | rs201954387 |
PheGenI | rs201954387 |
Biobank | rs201954387 |
1000 genomes | rs201954387 |
hgdp | rs201954387 |
ensembl | rs201954387 |
geneview | rs201954387 |
scholar | rs201954387 |
rs201954387 | |
pharmgkb | rs201954387 |
gwascentral | rs201954387 |
openSNP | rs201954387 |
23andMe | rs201954387 |
SNPshot | rs201954387 |
SNPdbe | rs201954387 |
MSV3d | rs201954387 |
GWAS Ctlg | rs201954387 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs201954387(A;A) |
Alt | rs201954387(A;A) |
Reference | Rs201954387(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | ACSF3 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000016.9:g.89212452G>A |
CLNSRC | |
CLNACC | RCV000426583.1, |