rs1064793662
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(AC;AC) | 0 | common in clinvar |
Chromosome | 16 |
Position | 89145346 |
Gene | ACSF3 |
is a | snp |
is | mentioned by |
dbSNP | rs1064793662 |
dbSNP (classic) | rs1064793662 |
ClinGen | rs1064793662 |
ebi | rs1064793662 |
HLI | rs1064793662 |
Exac | rs1064793662 |
Gnomad | rs1064793662 |
Varsome | rs1064793662 |
LitVar | rs1064793662 |
Map | rs1064793662 |
PheGenI | rs1064793662 |
Biobank | rs1064793662 |
1000 genomes | rs1064793662 |
hgdp | rs1064793662 |
ensembl | rs1064793662 |
geneview | rs1064793662 |
scholar | rs1064793662 |
rs1064793662 | |
pharmgkb | rs1064793662 |
gwascentral | rs1064793662 |
openSNP | rs1064793662 |
23andMe | rs1064793662 |
SNPshot | rs1064793662 |
SNPdbe | rs1064793662 |
MSV3d | rs1064793662 |
GWAS Ctlg | rs1064793662 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1064793662(-;-) |
Alt | rs1064793662(-;-) |
Reference | Rs1064793662(AC;AC) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | ACSF3 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000016.9:g.89211754_89211755delCA |
CLNSRC | |
CLNACC | RCV000480293.1, |