rs797044801
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs797044801(A;C) |
Make rs797044801(C;C) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 16 |
Position | 70254688 |
Gene | AARS |
is a | snp |
is | mentioned by |
dbSNP | rs797044801 |
dbSNP (classic) | rs797044801 |
ClinGen | rs797044801 |
ebi | rs797044801 |
HLI | rs797044801 |
Exac | rs797044801 |
Gnomad | rs797044801 |
Varsome | rs797044801 |
LitVar | rs797044801 |
Map | rs797044801 |
PheGenI | rs797044801 |
Biobank | rs797044801 |
1000 genomes | rs797044801 |
hgdp | rs797044801 |
ensembl | rs797044801 |
geneview | rs797044801 |
scholar | rs797044801 |
rs797044801 | |
pharmgkb | rs797044801 |
gwascentral | rs797044801 |
openSNP | rs797044801 |
23andMe | rs797044801 |
SNPshot | rs797044801 |
SNPdbe | rs797044801 |
MSV3d | rs797044801 |
GWAS Ctlg | rs797044801 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs797044801(C;C) |
Alt | rs797044801(C;C) |
Reference | Rs797044801(A;A) |
Significance | Pathogenic |
Disease | Charcot-Marie-Tooth disease |
Variation | info |
Gene | AARS |
CLNDBN | Charcot-Marie-Tooth disease |
Reversed | 1 |
HGVS | NC_000016.9:g.70288591T>G |
CLNSRC | |
CLNACC | RCV000192254.1, |