rs766771165
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
Make rs766771165(-;A) |
Make rs766771165(A;A) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 6 |
Position | 44307280 |
Gene | AARS2 |
is a | snp |
is | mentioned by |
dbSNP | rs766771165 |
dbSNP (classic) | rs766771165 |
ClinGen | rs766771165 |
ebi | rs766771165 |
HLI | rs766771165 |
Exac | rs766771165 |
Gnomad | rs766771165 |
Varsome | rs766771165 |
LitVar | rs766771165 |
Map | rs766771165 |
PheGenI | rs766771165 |
Biobank | rs766771165 |
1000 genomes | rs766771165 |
hgdp | rs766771165 |
ensembl | rs766771165 |
geneview | rs766771165 |
scholar | rs766771165 |
rs766771165 | |
pharmgkb | rs766771165 |
gwascentral | rs766771165 |
openSNP | rs766771165 |
23andMe | rs766771165 |
SNPshot | rs766771165 |
SNPdbe | rs766771165 |
MSV3d | rs766771165 |
GWAS Ctlg | rs766771165 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs766771165(A;A) |
Alt | rs766771165(A;A) |
Reference | Rs766771165(-;-) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | AARS2 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000006.11:g.44275018dupA |
CLNSRC | |
CLNACC | RCV000199735.1, |