rs775065697
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs775065697(A;G) |
Make rs775065697(G;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 6 |
Position | 44303159 |
Gene | AARS2 |
is a | snp |
is | mentioned by |
dbSNP | rs775065697 |
dbSNP (classic) | rs775065697 |
ClinGen | rs775065697 |
ebi | rs775065697 |
HLI | rs775065697 |
Exac | rs775065697 |
Gnomad | rs775065697 |
Varsome | rs775065697 |
LitVar | rs775065697 |
Map | rs775065697 |
PheGenI | rs775065697 |
Biobank | rs775065697 |
1000 genomes | rs775065697 |
hgdp | rs775065697 |
ensembl | rs775065697 |
geneview | rs775065697 |
scholar | rs775065697 |
rs775065697 | |
pharmgkb | rs775065697 |
gwascentral | rs775065697 |
openSNP | rs775065697 |
23andMe | rs775065697 |
SNPshot | rs775065697 |
SNPdbe | rs775065697 |
MSV3d | rs775065697 |
GWAS Ctlg | rs775065697 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs775065697(G;G) |
Alt | rs775065697(G;G) |
Reference | Rs775065697(A;A) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | AARS2 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000006.11:g.44270896A>G |
CLNSRC | |
CLNACC | RCV000196157.1, |